Canonical Allele Identifier: PA916027892
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 31191
ClinVar RCV Id: RCV000024190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317210.1:p.Tyr72Cys
CA260012
NM_001330281.2:c.215A>G