Canonical Allele Identifier: PA2828775988
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375947
ClinVar RCV Id: RCV000417560 RCV000420810 RCV000428250 RCV000433859 RCV000423137 RCV000441525 RCV000428467 RCV000430625 RCV000435646 RCV000441346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Asp594His
CA16602426
NM_001378468.1:c.1780G>C