Allele Registry

Canonical Allele Identifier: PA2573078013

Gene: KIT HGNC NCBI

ClinVar RCV:

RCV000421498

ClinVar Variation:

376058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372219.1:p.Thr671Ile	CA16602525 NM_001385290.1:c.2012C>T