Canonical Allele Identifier: PA218571
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66964
ClinVar RCV Id: RCV000057497
ClinVar Variation Id: 66965
ClinVar RCV Id: RCV000057498 RCV000790002 RCV001854179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Glu33Asp
CA018946
NM_170707.4:c.99G>C
CA018951
NM_170707.4:c.99G>T