Allele Registry

Canonical Allele Identifier: PA2828966098

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000428828

ClinVar Variation:

376736

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372214.1:p.Trp557Phe	CA16603144 NM_001385285.1:c.1670_1671delinsTT