Canonical Allele Identifier: PA658682072
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 463833
ClinVar RCV Id: RCV000536078 RCV002438352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Ala34Thr
CA347656115
NM_017849.4:c.100G>A