Canonical Allele Identifier: PA2825091951
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 840297
ClinVar RCV Id: RCV001042251

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Ser453Ala
CA356906229
NM_000222.3:c.1357T>G