Canonical Allele Identifier: PA103492
Gene: TMEM165 HGNC NCBI

Linked Data

ClinVar Variation Id: 35520
ClinVar RCV Id: RCV000029181 RCV002251428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060945.2:p.Arg126Cys
CA260080
NM_018475.5:c.376C>T