Canonical Allele Identifier: PA2826176307
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 960997
ClinVar RCV Id: RCV001234621 RCV002451562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.His120Arg
CA1777345
NM_001193304.3:c.359A>G