Canonical Allele Identifier: PA2829594708
Gene: HSPG2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005520.4:p.Lys1407Arg
CA338958262
NM_005529.7:c.4220A>G