Allele Registry

Canonical Allele Identifier: PA2829021903

Gene: KIT HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000014864

RCV000431704

RCV000443179

RCV000444150

RCV000505554

RCV000656673

RCV000656674

RCV000656675

RCV000656676

RCV001269832

RCV002453261

ClinVar Variation:

13852

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372219.1:p.Asp816Val	CA123513 NM_001385290.1:c.2447A>T CA2850447376 NM_001385290.1:c.2447_2448delinsTT