Canonical Allele Identifier: PA645488802
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 409757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Asn828Asp
CA16611682
NM_000222.3:c.2482A>G