Canonical Allele Identifier: PA2828775826
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711054
ClinVar RCV Id: RCV002292341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Pro453Leu
CA369588964
NM_001378468.1:c.1358C>T