Canonical Allele Identifier: PA2825455906
Gene: TMEM134 HGNC NCBI

Linked Data

ClinVar Variation Id: 2327628
ClinVar RCV Id: RCV004167845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001072119.1:p.Ser81Pro
CA381539651
NM_001078651.3:c.241T>C