Canonical Allele Identifier: PA645418326
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 305067
ClinVar RCV Id: RCV000407594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057548.1:p.Arg161Gln
CA6034671
NM_016464.5:c.482G>A