Canonical Allele Identifier: PA129934
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 35502
ClinVar RCV Id: RCV000029170
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Val620Ala
CA129932
NM_000222.3:c.1859T>C