Canonical Allele Identifier: PA200632
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 193507
ClinVar RCV Id: RCV000173581 RCV000860917 RCV000988093 RCV001704249 RCV002485119 RCV004539599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Val9Met
CA200630
NM_153704.6:c.25G>A