Canonical Allele Identifier: PA2829374315
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 578311
ClinVar RCV Id: RCV000701278 RCV001561766 RCV002332480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002285.1:p.Asn148Ser
CA10505302
NM_002294.3:c.443A>G