Allele Registry

Canonical Allele Identifier: PA2829018484

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000438560

ClinVar Variation:

376731

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372215.1:p.Trp553Ser	CA16603139 NM_001385286.1:c.1658G>C