Canonical Allele Identifier: PA110356
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 126963
ClinVar RCV Id: RCV000114821 RCV001012328 RCV000542243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Trp53Ser
CA269737
NM_001193304.3:c.158G>C