Canonical Allele Identifier: PA2830325764
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 644974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Thr24Ser
CA342807227
NM_170707.4:c.70A>T
CA342807231
NM_170707.4:c.71C>G