Canonical Allele Identifier: PA111976
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13843
ClinVar RCV Id: RCV000014855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Gly664Arg
CA123500
NM_000222.3:c.1990G>A
CA356908804
NM_000222.3:c.1990G>C