Canonical Allele Identifier: PA645423559
Gene: TMEM47 HGNC NCBI

Linked Data

ClinVar Variation Id: 242889
ClinVar RCV Id: RCV000491018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113630.1:p.Arg12Pro
CA412682009
NM_031442.4:c.35G>C