Canonical Allele Identifier: PA2826659436
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2831707
ClinVar RCV Id: RCV003744337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Met540Lys
CA342825341
NM_001282625.2:c.1619T>A