Canonical Allele Identifier: PA2828775249
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_001365396.1:p.His577Gln
CA281986
NM_001378467.1:c.1731C>G
CA295914
NM_001378467.1:c.1731C>A