Canonical Allele Identifier: PA2825843014
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356294
ClinVar RCV Id: RCV001880392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Met171Ile
CA371687777
NM_001142301.1:c.513G>T
CA371687778
NM_001142301.1:c.513G>C
CA371687779
NM_001142301.1:c.513G>A