Canonical Allele Identifier: PA2742012012
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 2921894
ClinVar RCV Id: RCV003782916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Met252Val
CA371687773
NM_153704.6:c.754A>G