Canonical Allele Identifier: PA2828778591
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376292
ClinVar RCV Id: RCV000420521
ClinVar Variation Id: 376293
ClinVar RCV Id: RCV000431213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Asp535Glu
CA16602740
NM_001378472.1:c.1605C>G
CA16602741
NM_001378472.1:c.1605C>A