Canonical Allele Identifier: PA2828776021
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 41446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Lys601Gln
CA215454
NM_001378468.1:c.1801A>C