Allele Registry

Canonical Allele Identifier: PA2829018598

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV001312360

RCV002431880

ClinVar Variation:

1013731

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372215.1:p.Thr842Ala	CA356913175 NM_001385286.1:c.2524A>G