Canonical Allele Identifier: PA2826256729
Gene: FAM161A HGNC NCBI

Linked Data

ClinVar Variation Id: 336739
ClinVar RCV Id: RCV000309470 RCV000967952 RCV001699327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001188472.1:p.Arg338Gln
CA1679232
NM_001201543.2:c.1013G>A