Canonical Allele Identifier: PA2826658692
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14483
ClinVar RCV Id: RCV000015572 RCV000057425 RCV000211789 RCV000794743
ClinVar Variation Id: 66913
ClinVar RCV Id: RCV000057424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asn195Lys
CA018269
NM_001282625.2:c.585C>A
CA018275
NM_001282625.2:c.585C>G