Canonical Allele Identifier: PA2826176359
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 532503
ClinVar RCV Id: RCV000639331 RCV002331157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Cys140Phe
CA347653164
NM_001193304.3:c.419G>T