Canonical Allele Identifier: PA2826256557
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 336743
ClinVar RCV Id: RCV000388264 RCV000733680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188472.1:p.Gln118His
CA1679384
NM_001201543.2:c.354G>T
CA346989361
NM_001201543.2:c.354G>C