Canonical Allele Identifier: PA2826658004
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14478
ClinVar RCV Id: RCV000015565 RCV000057273 RCV000500734 RCV001095717 RCV000472112 RCV001813989 RCV003313922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg372Trp
CA017033
NM_001282624.2:c.1114C>T