Allele Registry

Canonical Allele Identifier: PA2829019958

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000421498

ClinVar Variation:

376058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372217.1:p.Thr667Ile	CA16602525 NM_001385288.1:c.2000C>T