Allele Registry

Canonical Allele Identifier: PA2573077997

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000029170

ClinVar Variation:

35502

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372219.1:p.Val621Ala	CA129932 NM_001385290.1:c.1862T>C