Canonical Allele Identifier: PA102701
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217726
ClinVar RCV Id: RCV000201528 RCV000419395 RCV000636949 RCV002478718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Thr372Lys
CA279345
NM_153704.6:c.1115C>A