Allele Registry

Canonical Allele Identifier: PA2828970190

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000423846

RCV000441099

ClinVar Variation:

375905

375906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372215.1:p.Lys546Asn	CA16602388 NM_001385286.1:c.1638A>C CA16602389 NM_001385286.1:c.1638A>T