Allele Registry

Canonical Allele Identifier: PA645488371

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000438326

RCV000701684

ClinVar Variation:

375922

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Asn655Ser	CA16602403 NM_000222.3:c.1964A>G