Canonical Allele Identifier: PA2828776613
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40384
ClinVar Variation Id: 180788
ClinVar RCV Id: RCV000157823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.His552Gln
CA281986
NM_001378469.1:c.1656C>G
CA295914
NM_001378469.1:c.1656C>A