Canonical Allele Identifier: PA2830325908
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 246300
ClinVar RCV Id: RCV000235498
ClinVar Variation Id: 1709835
ClinVar RCV Id: RCV002290177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Val49Leu
CA10584110
NM_170707.4:c.145G>C
CA342807952
NM_170707.4:c.145G>T