Canonical Allele Identifier: PA277769
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217721
ClinVar RCV Id: RCV000201683 RCV002222442 RCV001853242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Arg91Gln
CA277766
NM_001142301.1:c.272G>A