Canonical Allele Identifier: PA2826660822
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245639
ClinVar RCV Id: RCV000727363 RCV001079513 RCV001184766 RCV002418036 RCV003998896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asn610Asp
CA051914
NM_001282626.2:c.1828A>G