Canonical Allele Identifier: PA144486
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 56780
ClinVar RCV Id: RCV000050193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Leu885Pro
CA144483
NM_001142301.1:c.2654T>C