Canonical Allele Identifier: PA2826176142
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 1518446
ClinVar RCV Id: RCV002043473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.His57Gln
CA347655971
NM_001193304.3:c.171C>G
CA347655972
NM_001193304.3:c.171C>A