Canonical Allele Identifier: PA645476148
Gene: TMEM165 HGNC NCBI

Linked Data

ClinVar Variation Id: 349067
ClinVar RCV Id: RCV000262152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060945.2:p.Asp201Gly
CA2925538
NM_018475.5:c.602A>G