Canonical Allele Identifier: PA167274
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 142056
ClinVar RCV Id: RCV000130864 RCV000415718 RCV000466516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.His133Arg
CA167272
NM_017849.4:c.398A>G