Canonical Allele Identifier: PA2826176537
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014859
ClinVar RCV Id: RCV001313649 RCV003166787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Tyr220His
CA347651492
NM_001193304.3:c.658T>C