Canonical Allele Identifier: PA2827293344
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 287964
ClinVar RCV Id: RCV000320558 RCV000350217 RCV002521986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317210.1:p.Ile25Val
CA6034560
NM_001330281.2:c.73A>G