Canonical Allele Identifier: PA2825842993
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 449519
ClinVar RCV Id: RCV000519954 RCV001165120 RCV001165118 RCV001165119 RCV001333011 RCV001198569 RCV001797744 RCV002476053 RCV001857955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Gly137Ala
CA4807740
NM_001142301.1:c.410G>C