Canonical Allele Identifier: PA645488267
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 375919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Leu576Pro
CA16602401
NM_000222.3:c.1727T>C
CA891841855
NM_000222.3:c.1727_1731delinsCTCCC