Canonical Allele Identifier: PA1139755444
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 944956
ClinVar RCV Id: RCV001215471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ala539Val
CA342825326
NM_170707.4:c.1616C>T
CA2831039324
NM_170707.4:c.1616_1617delinsTT