Allele Registry

Canonical Allele Identifier: PA2829018588

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000439224

ClinVar Variation:

376101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372215.1:p.Tyr818Asp	CA16602561 NM_001385286.1:c.2452T>G