Canonical Allele Identifier: PA2827549305
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_001337460.1:p.Asp201Tyr
CA174878
NM_001350531.2:c.601G>T