Canonical Allele Identifier: PA2828966047
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 627637
ClinVar RCV Id: RCV000771008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372214.1:p.[Pro551_Val555del;Trp557_Lys558del]
CA913189819
NM_001385285.1:c.1652_1672del