Canonical Allele Identifier: PA102471
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Arg441Cys
CA277817
NM_153704.6:c.1321C>T