Canonical Allele Identifier: PA2825471435
Gene: FAM163B HGNC NCBI

Linked Data

ClinVar Variation Id: 3091961
ClinVar RCV Id: RCV004378820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073984.1:p.Met152Arg
CA5312850
NM_001080515.3:c.455T>G