Allele Registry

Canonical Allele Identifier: PA123518

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000014867

RCV001303922

ClinVar Variation:

13853

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Asp820Gly	CA123516 NM_000222.3:c.2459A>G