Canonical Allele Identifier: PA2826657877
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1052547
ClinVar RCV Id: RCV001360754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Pro310Ala
CA342820834
NM_001282624.2:c.928C>G