Canonical Allele Identifier: PA2830327785
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 502242
ClinVar RCV Id: RCV000593108 RCV001387373
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Asp446Gly
CA342822060
NM_170707.4:c.1337A>G