Canonical Allele Identifier: PA2826659347
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245964
ClinVar RCV Id: RCV000235878 RCV000653862 RCV000681642 RCV001100889 RCV001100614 RCV001100615 RCV001100616 RCV001100617 RCV001098789 RCV001100613 RCV001100618 RCV001100619 RCV001100620 RCV001180056 RCV002392729 RCV002494678 RCV003998908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Thr496Met
CA050321
NM_001282625.2:c.1487C>T