Canonical Allele Identifier: PA2828776514
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44802
ClinVar RCV Id: RCV000037918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gly447del
CA135082
NM_001378469.1:c.1339_1341del