Allele Registry

Canonical Allele Identifier: PA645488174

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000430398

ClinVar Variation:

375904

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Phe504Leu	CA16602387 NM_000222.3:c.1510T>C CA356906628 NM_000222.3:c.1512T>A CA356906630 NM_000222.3:c.1512T>G