Canonical Allele Identifier: PA2827158290
Gene: LMAN2L HGNC NCBI

Linked Data

ClinVar Variation Id: 1031876
ClinVar RCV Id: RCV001333824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309276.1:p.Asp132Val
CA347710247
NM_001322347.2:c.395A>T