Canonical Allele Identifier: PA102664
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217709
ClinVar RCV Id: RCV000201664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Pro130Arg
CA279467
NM_153704.6:c.389C>G