Canonical Allele Identifier: PA2829022764
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 375919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Leu573Pro
CA16602401
NM_001385292.1:c.1718T>C
CA891841855
NM_001385292.1:c.1718_1722delinsCTCCC