Canonical Allele Identifier: PA2826660785
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 162411
ClinVar RCV Id: RCV000192014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Cys591Ser
CA347053
NM_001282626.2:c.1771T>A
CA342826702
NM_001282626.2:c.1772G>C