Canonical Allele Identifier: PA2826659242
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 519022
ClinVar RCV Id: RCV000621062 RCV001096941 RCV001096943 RCV001096942 RCV001096944 RCV001096939 RCV001096940 RCV001102354 RCV001102355 RCV000808964 RCV001190252 RCV001096945 RCV001096946 RCV001544605 RCV004002668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Val442Met
CA049885
NM_001282625.2:c.1324G>A