Canonical Allele Identifier: PA277792
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 216826
ClinVar RCV Id: RCV000198666 RCV000201726 RCV000624166 RCV001090385 RCV002283466 RCV001814102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Asn161Ser
CA277789
NM_001142301.1:c.482A>G