Allele Registry

Canonical Allele Identifier: PA112058

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000014870

RCV000419360

ClinVar Variation:

13856

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Val559Asp	CA123522 NM_000222.3:c.1676T>A