Canonical Allele Identifier: PA223830
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 96216
ClinVar RCV Id: RCV000416124 RCV001138007 RCV001274720 RCV003952528
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188472.1:p.Gln385Glu
CA223829
NM_001201543.2:c.1153C>G