Canonical Allele Identifier: PA217888
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66802
ClinVar RCV Id: RCV000057265 RCV000150953 RCV000148606 RCV000653929 RCV001172619 RCV001524022 RCV002381364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg435Cys
CA014967
NM_005572.4:c.1303C>T