Canonical Allele Identifier: PA2573306424
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497085
ClinVar RCV Id: RCV002019339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Ile131Thr
CA371685916
NM_153704.6:c.392T>C