Canonical Allele Identifier: PA180035
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 167059
ClinVar RCV Id: RCV000153228 RCV000330220 RCV000954594 RCV001526760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115556.2:p.Thr66Ile
CA180033
NM_032180.3:c.197C>T