Canonical Allele Identifier: PA2742011992
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 2932474
ClinVar RCV Id: RCV003795688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Glu124Ala
CA371685862
NM_153704.6:c.371A>C