Canonical Allele Identifier: PA2826443971
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 643617
ClinVar RCV Id: RCV000797360 RCV001179798 RCV001007472 RCV004001610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.His454Asp
CA342825888
NM_001257374.3:c.1360C>G