Canonical Allele Identifier: PA2828778507
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1351912
ClinVar RCV Id: RCV002049339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Met432Ile
CA4516724
NM_001378472.1:c.1296G>A
CA369588482
NM_001378472.1:c.1296G>C
CA369588483
NM_001378472.1:c.1296G>T