Canonical Allele Identifier: PA2829839368
Gene: TMEM138 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401571
ClinVar RCV Id: RCV001912943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057548.1:p.Arg103Cys
CA6034589
NM_016464.5:c.307C>T