Allele Registry

Canonical Allele Identifier: PA223831

Gene: FAM161A HGNC NCBI

ClinVar RCV:

RCV000416124

RCV001138007

RCV001274720

RCV003952528

ClinVar Variation:

96216

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