Canonical Allele Identifier: PA233982
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 167058
ClinVar RCV Id: RCV000153227 RCV000765693 RCV001844052 RCV001138008 RCV003907444
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188472.1:p.Leu378Arg
CA233981
NM_001201543.2:c.1133T>G