Canonical Allele Identifier: PA2573267457
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522390
ClinVar RCV Id: RCV002046542
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057548.1:p.Ser5Gly
CA380677420
NM_016464.5:c.13A>G