Allele Registry

Canonical Allele Identifier: PA645488377

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000421498

ClinVar Variation:

376058

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Thr670Ile	CA16602525 NM_000222.3:c.2009C>T