Canonical Allele Identifier: PA277792
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 216826

Amino-acid Alleles

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