Allele Registry

Canonical Allele Identifier: PA102574

Gene: TMEM67 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

16417

ClinVar RCV:

RCV000001445

RCV000001446

RCV000821785

RCV000995902

RCV001310635

RCV001536092

RCV001804708

RCV003315221

ClinVar Variation:

1378

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_714915.3:p.Ile833Thr	CA210657 NM_153704.6:c.2498T>C