Canonical Allele Identifier: PA2573267464
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501736
ClinVar RCV Id: RCV002019895
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057548.1:p.Ser28Ala
CA6034514
NM_016464.5:c.82T>G