Canonical Allele Identifier: PA210660
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378
ClinVar RCV Id: RCV000001445 RCV000001446 RCV000995902 RCV000821785 RCV001310635 RCV001536092 RCV001804708 RCV003315221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Ile752Thr
CA210657
NM_001142301.1:c.2255T>C