Canonical Allele Identifier: PA2826657896
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14519
ClinVar RCV Id: RCV001174241 RCV000653937 RCV001257937 RCV001188431 RCV002336085 RCV000015616 RCV000057255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg318Cys
CA016847
NM_001282624.2:c.952C>T