Canonical Allele Identifier: PA2826660189
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48092
ClinVar RCV Id: RCV000041378 RCV000148604 RCV000619864 RCV000726532 RCV000777745 RCV001086902 RCV001174244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ile299Val
CA014949
NM_001282626.2:c.895A>G