Canonical Allele Identifier: PA2830326320
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1471137
ClinVar RCV Id: RCV001995389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Phe113Leu
CA342808869
NM_170707.4:c.337T>C
CA342808874
NM_170707.4:c.339T>G
CA342808875
NM_170707.4:c.339T>A