Allele Registry

Canonical Allele Identifier: PA645488222

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000439662

ClinVar Variation:

376734

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Trp557Cys	CA16603142 NM_000222.3:c.1671G>C CA356907466 NM_000222.3:c.1671G>T