Canonical Allele Identifier: PA2741837558
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630676
ClinVar RCV Id: RCV004539031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Leu3Val
CA371685895
NM_001142301.1:c.7C>G