Canonical Allele Identifier: PA2829020309
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1369437
ClinVar RCV Id: RCV001870631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Glu846Asp
CA356913227
NM_001385288.1:c.2538A>C
CA356913228
NM_001385288.1:c.2538A>T