Canonical Allele Identifier: PA916027891
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 31189
ClinVar RCV Id: RCV000024188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317210.1:p.Ala69Val
CA260010
NM_001330281.2:c.206C>T