Canonical Allele Identifier: PA2830308119
Gene: FAM161B HGNC NCBI

Linked Data

ClinVar Variation Id: 136986
ClinVar RCV Id: RCV000124550 RCV001198189 RCV003965043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689658.2:p.Pro28Leu
CA290442
NM_152445.2:c.83C>T