Canonical Allele Identifier: PA2829603693
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2894607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Ser390Phe
CA342820822
NM_005572.4:c.1169C>T