Canonical Allele Identifier: PA172477
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66952
ClinVar RCV Id: RCV000057481 RCV000146262 RCV001234965 RCV003227631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Asp300Asn
CA018826
NM_170707.4:c.898G>A