Canonical Allele Identifier: PA2826658207
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 926250
ClinVar RCV Id: RCV001188738 RCV001237588 RCV004010302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp474Gly
CA31014778
NM_001282624.2:c.1421A>G