Canonical Allele Identifier: PA658659274
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 472885
ClinVar RCV Id: RCV000551567
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057548.1:p.Val65Ile
CA6034557
NM_016464.5:c.193G>A