Canonical Allele Identifier: PA2830329223
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1705143
ClinVar RCV Id: RCV002281773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Met200Ile
CA342817007
NM_170708.4:c.600G>A
CA342817008
NM_170708.4:c.600G>C
CA342817009
NM_170708.4:c.600G>T