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CCT5 c.1620A>C ;(p.E540D)
Variant ID: 5-10264889-A-C
NM_012073.3(
CCT5
):c.1620A>C;(p.E540D)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications: