Canonical Allele Identifier: PA2829603002
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1471137
ClinVar RCV Id: RCV001995389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Phe113Leu
CA342808869
NM_005572.4:c.337T>C
CA342808874
NM_005572.4:c.339T>G
CA342808875
NM_005572.4:c.339T>A