Canonical Allele Identifier: PA2828775858
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13971
ClinVar RCV Id: RCV000015005 RCV000150210 RCV000419278 RCV000422572 RCV000421485 RCV000430006 RCV000432193 RCV000432393 RCV000439564 RCV000444131 RCV000440864 RCV000439801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Gly469Ala
CA123655
NM_001378468.1:c.1406G>C