Canonical Allele Identifier: PA645453408
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 266099
ClinVar RCV Id: RCV000256415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Glu903Gln
CA10588966
NM_153704.6:c.2707G>C