Canonical Allele Identifier: PA102621
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217710
ClinVar RCV Id: RCV000201614 RCV002517316 RCV002500631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Met257Val
CA279411
NM_153704.6:c.769A>G