Canonical Allele Identifier: PA2826176379
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 2496964
ClinVar RCV Id: RCV003216541 RCV003517470 RCV003966293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180233.1:p.Ala150Pro
CA347653000
NM_001193304.3:c.448G>C