Canonical Allele Identifier: PA215589
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Gly565Val
CA215587
NM_000222.3:c.1694G>T