Canonical Allele Identifier: PA645452700
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 411582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Gly75Glu
CA4807559
NM_153704.6:c.224G>A