Canonical Allele Identifier: PA2828778585
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44811
ClinVar RCV Id: RCV000037929 RCV000524048 RCV000763165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Asn529Lys
CA280022
NM_001378472.1:c.1587T>A
CA369543395
NM_001378472.1:c.1587T>G