BRAF c.1798_1799insAGGCAACAG ;(p.T599_V600insEAT)

Variant ID: 7-140453136-A-ACTGTTGCCT

NM_004333.4(BRAF):c.1798_1799insAGGCAACAG;(p.T599_V600insEAT)

This variant was identified in 1 publication

View GRCh38 version.




Publications: