Canonical Allele Identifier: PA2828967387
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13861
ClinVar RCV Id: RCV000014875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372214.1:p.Thr846Pro
CA123535
NM_001385285.1:c.2536A>C