Canonical Allele Identifier: PA916058047
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 646591
ClinVar RCV Id: RCV000800910 RCV001012880 RCV003478500 RCV003461124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Gly58Arg
CA1777386
NM_017849.4:c.172G>A
CA347655970
NM_017849.4:c.172G>C