Canonical Allele Identifier: PA233983
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 167058
ClinVar RCV Id: RCV000153227 RCV000765693 RCV001844052 RCV001138008 RCV003907444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115556.2:p.Leu378Arg
CA233981
NM_032180.3:c.1133T>G