Canonical Allele Identifier: PA117664
Gene: CST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 5635
ClinVar RCV Id: RCV000005989 RCV002054421 RCV002490325 RCV001777132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000090.1:p.Ala25Thr
CA117663
NM_000099.4:c.73G>A