Canonical Allele Identifier: PA102556
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1382
ClinVar RCV Id: RCV000001450 RCV000587331
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Gly821Ser
CA114973
NM_153704.6:c.2461G>A