Canonical Allele Identifier: PA2580522488
Gene: FAM161B HGNC NCBI

Linked Data

ClinVar Variation Id: 2220231
ClinVar RCV Id: RCV004089672
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689658.3:p.Tyr226His
CA263562396
NM_152445.3:c.676T>C