Canonical Allele Identifier: PA2825842993
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 449519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Gly137Ala
CA4807740
NM_001142301.1:c.410G>C