Canonical Allele Identifier: PA2826176130
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1776107
ClinVar RCV Id: RCV002398624 RCV003100742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Trp53Cys
CA1777388
NM_001193304.3:c.159G>T
CA347655999
NM_001193304.3:c.159G>C