Allele Registry

Canonical Allele Identifier: PA211568

Gene: KIT HGNC NCBI

ClinVar Allele:

171097

ClinVar RCV:

RCV000148560

RCV000514124

RCV001023936

RCV001079840

RCV003952706

ClinVar Variation:

161259

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Ala178Thr	CA211566 NM_000222.3:c.532G>A