Canonical Allele Identifier: PA2828777348
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375940
ClinVar RCV Id: RCV000440177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Val566Arg
CA16021333
NM_001378470.1:c.1696_1697delinsAG
CA645544098
NM_001378470.1:c.1696_1697delinsCG
CA645544099
NM_001378470.1:c.1695_1697delinsGAG