Canonical Allele Identifier: PA144503
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 56788
ClinVar RCV Id: RCV000050201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Ser245Phe
CA144499
NM_153704.6:c.734C>T