Canonical Allele Identifier: PA102652
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217722
ClinVar RCV Id: RCV000201774 RCV001753605
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Phe942Cys
CA279557
NM_153704.6:c.2825T>G