Canonical Allele Identifier: PA114988
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1385
ClinVar RCV Id: RCV000001455 RCV000001454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Gly740Arg
CA114985
NM_001142301.1:c.2218G>C