Canonical Allele Identifier: PA114984
Gene: TMEM67 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384
ClinVar RCV Id: RCV000001453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135773.1:p.Trp209Leu
CA114981
NM_001142301.1:c.626G>T