Canonical Allele Identifier: PA891863656
Gene: SRPX2 HGNC NCBI
ClinVar RCV:
RCV000723306
ClinVar Variation:
592112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055282.1:p.Pro187Leu
CA413933775
NM_014467.3:c.560C>T