Canonical Allele Identifier: PA2826659544
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 644974
ClinVar RCV Id: RCV000798982 RCV002370101 RCV003532266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr24Ser
CA342807227
NM_001282626.2:c.70A>T
CA342807231
NM_001282626.2:c.71C>G