Canonical Allele Identifier: PA215592
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Ala755Thr
CA215590
NM_000222.3:c.2263G>A