Canonical Allele Identifier: PA142492
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48056
ClinVar RCV Id: RCV000041338 RCV000725381 RCV001084443 RCV001188113 RCV004541209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Gly638Arg
CA015346
NM_170707.4:c.1912G>A
CA342827858
NM_170707.4:c.1912G>C