Canonical Allele Identifier: PA2826250748
Gene: SIAE HGNC NCBI

Linked Data

ClinVar Variation Id: 2959501
ClinVar RCV Id: RCV003811676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186851.1:p.Thr449Met
CA6341170
NM_001199922.2:c.1346C>T