Canonical Allele Identifier: PA2828491830
Gene: FAM163B HGNC NCBI

Linked Data

ClinVar Variation Id: 3091961
ClinVar RCV Id: RCV004378820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358458.1:p.Met152Arg
CA5312850
NM_001371529.1:c.455T>G