Canonical Allele Identifier: PA2829889289
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2740622
ClinVar RCV Id: RCV003516679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Phe101Ser
CA347653521
NM_017849.4:c.302T>C