Canonical Allele Identifier: PA2826176118
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773131
ClinVar RCV Id: RCV002396705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Ala49Pro
CA347656029
NM_001193304.3:c.145G>C