Canonical Allele Identifier: PA102459
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 56764
ClinVar RCV Id: RCV000050177 RCV000430117 RCV001804788 RCV001853069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_714915.3:p.Arg440Gln
CA144435
NM_153704.6:c.1319G>A