Canonical Allele Identifier: PA2828780370
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711053
ClinVar RCV Id: RCV002292340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Val371Gly
CA369588924
NM_001378475.1:c.1112T>G