Canonical Allele Identifier: PA2826657809
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 242000
ClinVar RCV Id: RCV000227450 RCV000313924 RCV003165656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp283Asn
CA10581729
NM_001282624.2:c.847G>A