Allele Registry

Canonical Allele Identifier: PA2829021937

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000421785

RCV000428554

ClinVar Variation:

375933

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372219.1:p.Ala829Pro	CA16602413 NM_001385290.1:c.2485G>C