Allele Registry

Canonical Allele Identifier: PA2829958671

Gene: TMEM181 HGNC NCBI

ClinVar RCV:

RCV004072415

ClinVar Variation:

2204988

HGVS (amino-acid)	Matching Registered Transcripts
NP_065874.2:p.Tyr452Cys	CA4073610 NM_020823.2:c.1355A>G