Canonical Allele Identifier: PA2830327448
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 941172
ClinVar RCV Id: RCV001210900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Glu383Asp
CA342820648
NM_170707.4:c.1149G>C
CA342820650
NM_170707.4:c.1149G>T