Canonical Allele Identifier: PA2830328070
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2132526
ClinVar RCV Id: RCV003056055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ser507Arg
CA342823116
NM_170707.4:c.1519A>C
CA342823129
NM_170707.4:c.1521C>A
CA342823132
NM_170707.4:c.1521C>G