Canonical Allele Identifier: PA248399
Gene: TMEM72 HGNC NCBI

Linked Data

ClinVar Variation Id: 156705
ClinVar RCV Id: RCV000190283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116848.1:p.Ala138Asp
CA248398
NM_001123376.3:c.413C>A