Canonical Allele Identifier: PA2830058479
Gene: LMAN2L HGNC NCBI

Linked Data

ClinVar Variation Id: 1031876
ClinVar RCV Id: RCV001333824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110432.1:p.Asp259Val
CA347710247
NM_030805.4:c.776A>T