Allele Registry

Canonical Allele Identifier: PA2573239439

Gene: PRG4 HGNC NCBI

ClinVar RCV:

RCV002227894

ClinVar Variation:

1679878

HGVS (amino-acid)	Matching Registered Transcripts
NP_005798.3:p.Lys1212Asn	CA343954738 NM_005807.6:c.3636G>C CA343954747 NM_005807.6:c.3636G>T