Allele Registry

Canonical Allele Identifier: PA2829022693

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000438560

ClinVar Variation:

376731

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372221.1:p.Trp554Ser	CA16603139 NM_001385292.1:c.1661G>C