Canonical Allele Identifier: PA2829603134
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 854622
ClinVar RCV Id: RCV001059707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Lys171Asn
CA342815735
NM_005572.4:c.513G>C
CA342815737
NM_005572.4:c.513G>T