Allele Registry

Canonical Allele Identifier: PA2829019739

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000439662

ClinVar Variation:

376734

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372217.1:p.Trp554Cys	CA16603142 NM_001385288.1:c.1662G>C CA356907466 NM_001385288.1:c.1662G>T