Allele Registry

Canonical Allele Identifier: PA645488239

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000426761

RCV000436995

ClinVar Variation:

376056

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Val559Ile	CA16602523 NM_000222.3:c.1675G>A