Canonical Allele Identifier: PA2580522496
Gene: FAM161B HGNC NCBI

Linked Data

ClinVar Variation Id: 2235249
ClinVar RCV Id: RCV004092526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689658.3:p.Ala406Thr
CA7263626
NM_152445.3:c.1216G>A