Canonical Allele Identifier: PA279513
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217719
ClinVar RCV Id: RCV000201732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Gln295Glu
CA279510
NM_001142301.1:c.883C>G