Allele Registry

Canonical Allele Identifier: PA2829018487

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000421211

RCV000425331

RCV000431900

RCV000432558

RCV000442970

RCV002402117

ClinVar Variation:

375908

375909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372215.1:p.Trp553Arg	CA16602391 NM_001385286.1:c.1657T>A CA16602392 NM_001385286.1:c.1657T>C