Canonical Allele Identifier: PA2826176104
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 463837
ClinVar RCV Id: RCV000528885 RCV003114660 RCV001010941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Cys45Ser
CA52419092
NM_001193304.3:c.133T>A
CA347656049
NM_001193304.3:c.134G>C