Canonical Allele Identifier: PA2828969899
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 409756
ClinVar RCV Id: RCV000461759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Ser451Phe
CA16611498
NM_001385286.1:c.1352C>T