Canonical Allele Identifier: PA2828776022
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 376287
ClinVar RCV Id: RCV000432391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Lys601del
CA16602735
NM_001378468.1:c.1801_1803del
CA369543042
NM_001378468.1:c.1801A>T