Canonical Allele Identifier: PA223831
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 96216
ClinVar RCV Id: RCV000416124 RCV001138007 RCV001274720 RCV003952528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115556.2:p.Gln385Glu
CA223829
NM_032180.3:c.1153C>G