Canonical Allele Identifier: PA658682080
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 463838
ClinVar RCV Id: RCV000534477 RCV001011202 RCV003322782 RCV003392381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Thr46Ala
CA1777392
NM_017849.4:c.136A>G