Canonical Allele Identifier: PA112022
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13864
ClinVar RCV Id: RCV000014878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Phe584Cys
CA123543
NM_000222.3:c.1751T>G