Canonical Allele Identifier: PA2826176149
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2769496
ClinVar RCV Id: RCV003517784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Gly59Asp
CA347655962
NM_001193304.3:c.176G>A