Allele Registry

Canonical Allele Identifier: PA645488223

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000438560

ClinVar Variation:

376731

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Trp557Ser	CA16603139 NM_000222.3:c.1670G>C