Canonical Allele Identifier: PA645394502
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241838
ClinVar RCV Id: RCV000227816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612370.3:p.Gly644Cys
CA5247205
NM_138361.5:c.1930G>T