Allele Registry

Canonical Allele Identifier: PA2826878835

Gene: PRG4 HGNC NCBI

ClinVar RCV:

RCV002227894

ClinVar Variation:

1679878

HGVS (amino-acid)	Matching Registered Transcripts
NP_001290161.1:p.Lys1169Asn	CA343954738 NM_001303232.2:c.3507G>C CA343954747 NM_001303232.2:c.3507G>T