Canonical Allele Identifier: PA2742012857
Gene: FAM161B HGNC NCBI

Linked Data

ClinVar Variation Id: 2615761
ClinVar RCV Id: RCV004358822
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689658.3:p.Glu263Lys
CA390366659
NM_152445.3:c.787G>A