Canonical Allele Identifier: PA279437
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 217718
ClinVar RCV Id: RCV000201638
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.His790Asn
CA279433
NM_153704.6:c.2368C>A