Allele Registry

Canonical Allele Identifier: PA129934

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000029170

ClinVar Variation:

35502

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Val620Ala	CA129932 NM_000222.3:c.1859T>C