Canonical Allele Identifier: PA272897
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 161291
ClinVar RCV Id: RCV000148599 RCV000182377 RCV000245708 RCV000769735 RCV000725647 RCV001079490 RCV001330501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg644His
CA014889
NM_170707.4:c.1931G>A