Canonical Allele Identifier: PA2826660509
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 502242
ClinVar RCV Id: RCV000593108 RCV001387373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp446Gly
CA342822060
NM_001282626.2:c.1337A>G