Allele Registry

Canonical Allele Identifier: PA2829018486

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000439662

ClinVar Variation:

376734

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372215.1:p.Trp553Cys	CA16603142 NM_001385286.1:c.1659G>C CA356907466 NM_001385286.1:c.1659G>T