Canonical Allele Identifier: PA2826657886
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66792
ClinVar RCV Id: RCV000057253 RCV000157294 RCV001056678 RCV002336206 RCV002483088 RCV003996499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ser314Leu
CA016823
NM_001282624.2:c.941C>T