Canonical Allele Identifier: PA2829019552
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 2769232
ClinVar RCV Id: RCV003526556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Ser466Pro
CA356906303
NM_001385288.1:c.1396T>C