Canonical Allele Identifier: PA100317
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 31188
ClinVar RCV Id: RCV000024187 RCV000423402
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057548.1:p.His96Arg
CA260009
NM_016464.5:c.287A>G