Allele Registry

Canonical Allele Identifier: PA2829021927

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000439224

ClinVar Variation:

376101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372219.1:p.Tyr823Asp	CA16602561 NM_001385290.1:c.2467T>G