Canonical Allele Identifier: PA658813215
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 502242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Asp446Gly
CA342822060
NM_170708.4:c.1337A>G