Allele Registry

Canonical Allele Identifier: PA2573077958

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000439662

ClinVar Variation:

376734

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372219.1:p.Trp558Cys	CA16603142 NM_001385290.1:c.1674G>C CA356907466 NM_001385290.1:c.1674G>T