Canonical Allele Identifier: PA2826163916
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 472800
ClinVar RCV Id: RCV000546059 RCV002420508 RCV001507755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Arg677His
CA5247265
NM_001190723.3:c.2030G>A