Canonical Allele Identifier: PA2826657778
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2728396
ClinVar RCV Id: RCV003581262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Met271Thr
CA342820281
NM_001282624.2:c.812T>C