Canonical Allele Identifier: PA2828963182
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_001372213.1:p.[Pro552_Val556del;Trp558_Lys559del]
CA913189819
NM_001385284.1:c.1655_1675del