Canonical Allele Identifier: PA103839
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66819
ClinVar RCV Id: RCV000057286 RCV001060202 RCV001182565 RCV003996504 RCV002498332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Asp461Tyr
CA017154
NM_170707.4:c.1381G>T