Canonical Allele Identifier: PA2826660390
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66789
ClinVar RCV Id: RCV000057250 RCV001854173 RCV003992172 RCV003996498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg388Cys
CA016798
NM_001282626.2:c.1162C>T