Canonical Allele Identifier: PA2827883382
Gene: BRAF HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Lys483Asn
CA273507
NM_001354609.2:c.1449A>C
CA369588490
NM_001354609.2:c.1449A>T