Canonical Allele Identifier: PA2580509875
Gene: FAM3D HGNC NCBI

Linked Data

ClinVar Variation Id: 2375130
ClinVar RCV Id: RCV004215280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620160.1:p.Arg35Cys
CA2473088
NM_138805.3:c.103C>T