Canonical Allele Identifier: PA109354
Gene: PLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13574
ClinVar RCV Id: RCV000014542 RCV000490289 RCV002513047 RCV003317035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000292.1:p.Ala620Thr
CA123263
NM_000301.5:c.1858G>A