Canonical Allele Identifier: PA2580522500
Gene: FAM161B HGNC NCBI

Linked Data

ClinVar Variation Id: 2222316
ClinVar RCV Id: RCV004088140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689658.3:p.Ala529Val
CA7263498
NM_152445.3:c.1586C>T