Canonical Allele Identifier: PA2826660358
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 929053
ClinVar RCV Id: RCV001193914 RCV003480983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ala375Ser
CA342820537
NM_001282626.2:c.1123G>T