Canonical Allele Identifier: PA2826176415
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2784924
ClinVar RCV Id: RCV003633847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Gln168His
CA347652676
NM_001193304.3:c.504G>T
CA347652679
NM_001193304.3:c.504G>C