Canonical Allele Identifier: PA1139693532
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 962315
ClinVar RCV Id: RCV001236150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Lys41Gln
CA342814997
NM_001282624.2:c.121A>C