Canonical Allele Identifier: PA2830117018
Gene: LMLN HGNC NCBI

Linked Data

ClinVar Variation Id: 161526
ClinVar RCV Id: RCV000149061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149018.3:p.Gly365Cys
CA174267
NM_033029.4:c.1093G>T