Canonical Allele Identifier: PA1139670052
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 846369
ClinVar RCV Id: RCV001049662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Thr523Ala
CA356906947
NM_000222.3:c.1567A>G