Canonical Allele Identifier: PA2829603695
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_005563.1:p.Pro391Ala
CA342820834
NM_005572.4:c.1171C>G