Canonical Allele Identifier: PA102594
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 56780
ClinVar RCV Id: RCV000050193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Leu966Pro
CA144483
NM_153704.6:c.2897T>C