Canonical Allele Identifier: PA658682074
Gene: TMEM127 HGNC NCBI

Linked Data

ClinVar Variation Id: 480774
ClinVar RCV Id: RCV000574095 RCV000639355 RCV000760995 RCV002289801 RCV003153735 RCV003900253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060319.1:p.Ile41Val
CA1777395
NM_017849.4:c.121A>G