Canonical Allele Identifier: PA281988
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_004324.2:p.His574Gln
CA281986
NM_004333.6:c.1722C>G
CA295914
NM_004333.6:c.1722C>A