Canonical Allele Identifier: PA2828474935
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_001361173.1:p.Asp627Glu
CA16602740
NM_001374244.1:c.1881C>G
CA16602741
NM_001374244.1:c.1881C>A