Canonical Allele Identifier: PA645452564
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 363916
ClinVar RCV Id: RCV000302454 RCV000341063 RCV000397407 RCV002523703 RCV002488815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Ala10Val
CA4807496
NM_153704.6:c.29C>T