Allele Registry

Canonical Allele Identifier: PA112041

Gene: KIT HGNC NCBI

ClinVar Allele:

28900

ClinVar RCV:

RCV000014875

ClinVar Variation:

13861

HGVS (amino-acid)	Matching Registered Transcripts
NP_000213.1:p.Thr847Pro	CA123535 NM_000222.3:c.2539A>C