Canonical Allele Identifier: PA2573099630
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1314518
ClinVar RCV Id: RCV001773027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Thr108Ala
CA371685750
NM_153704.6:c.322A>G