Canonical Allele Identifier: PA2573306454
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520743
ClinVar RCV Id: RCV002030925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Thr244Ile
CA371687727
NM_153704.6:c.731C>T