Allele Registry

Canonical Allele Identifier: PA123542

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000014877

RCV000379347

RCV000418294

RCV000428990

RCV000439677

RCV000505647

ClinVar Variation:

13863

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Asp816His	CA123540 NM_000222.3:c.2446G>C CA645516949 NM_000222.3:c.2446_2448delinsCAT