Canonical Allele Identifier: PA2828777896
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1351912
ClinVar RCV Id: RCV002049339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365400.1:p.Met447Ile
CA4516724
NM_001378471.1:c.1341G>A
CA369588482
NM_001378471.1:c.1341G>C
CA369588483
NM_001378471.1:c.1341G>T