Canonical Allele Identifier: PA144491
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 56782
ClinVar RCV Id: RCV000050195 RCV002514271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Ser4Thr
CA144487
NM_001142301.1:c.10T>A