Canonical Allele Identifier: PA2828966167
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372214.1:p.Gly565Val
CA215587
NM_001385285.1:c.1694G>T