Canonical Allele Identifier: PA2828776484
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711785
ClinVar RCV Id: RCV002293330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gln434Leu
CA369588944
NM_001378469.1:c.1301A>T