Canonical Allele Identifier: PA2825842970
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 917961
ClinVar RCV Id: RCV001175228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Arg10Thr
CA371685957
NM_001142301.1:c.29G>C