Canonical Allele Identifier: PA2741837563
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 2503864
ClinVar RCV Id: RCV003230855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Trp6Cys
CA371685925
NM_001142301.1:c.18G>C
CA371685926
NM_001142301.1:c.18G>T