Canonical Allele Identifier: PA2828937582
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948931
ClinVar RCV Id: RCV001220288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371073.1:p.Pro402Ala
CA5247222
NM_001384144.1:c.1204C>G