Canonical Allele Identifier: PA2826657820
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2819423
ClinVar RCV Id: RCV003744174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Met290Ile
CA342820484
NM_001282624.2:c.870G>A
CA342820486
NM_001282624.2:c.870G>C
CA342820488
NM_001282624.2:c.870G>T