Canonical Allele Identifier: PA2829838724
Gene: LSR HGNC NCBI
ClinVar RCV:
RCV003825710
ClinVar Variation:
2965560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057009.4:p.Thr160Met
CA405286438
NM_015925.7:c.479C>T