Canonical Allele Identifier: PA2826660808
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48052
ClinVar RCV Id: RCV000041334 RCV000057361 RCV000148601 RCV000771799 RCV000617798 RCV001088263 RCV004541208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Gly602Ser
CA014839
NM_001282626.2:c.1804G>A