Canonical Allele Identifier: PA2828780367
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711785
ClinVar RCV Id: RCV002293330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Gln368Leu
CA369588944
NM_001378475.1:c.1103A>T