Canonical Allele Identifier: PA174879
Gene: LARP1B HGNC NCBI

Linked Data

ClinVar Variation Id: 161836
ClinVar RCV Id: RCV000149372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_835144.1:p.Asp442Tyr
CA174878
NM_178043.3:c.1324G>T