Canonical Allele Identifier: PA180032
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 167056
ClinVar RCV Id: RCV000153223 RCV000955288 RCV001140149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188472.1:p.Glu708Lys
CA180030
NM_001201543.2:c.2122G>A