Canonical Allele Identifier: PA2825843009
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520743
ClinVar RCV Id: RCV002030925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Thr163Ile
CA371687727
NM_001142301.1:c.488C>T