Canonical Allele Identifier: PA2741851766
Gene: HSPG2 HGNC NCBI
ClinVar RCV:
RCV003985012
ClinVar Variation:
3061970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278789.1:p.Lys1408Arg
CA338958262
NM_001291860.2:c.4223A>G