Canonical Allele Identifier: PA2826660750
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1329343
ClinVar RCV Id: RCV001799386 RCV003227992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ser571Asn
CA342826307
NM_001282626.2:c.1712G>A