Canonical Allele Identifier: PA2825843007
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1420116
ClinVar RCV Id: RCV001914030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Ala160Val
CA371687710
NM_001142301.1:c.479C>T