Canonical Allele Identifier: PA2573267464
Gene: TMEM138 HGNC NCBI
ClinVar RCV:
RCV002019895
ClinVar Variation:
1501736
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Amino-acid Alleles

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