Allele Registry

Canonical Allele Identifier: PA2825657768

Gene: PRG4 HGNC NCBI

ClinVar RCV:

RCV002227894

ClinVar Variation:

1679878

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121180.2:p.Lys1171Asn	CA343954738 NM_001127708.3:c.3513G>C CA343954747 NM_001127708.3:c.3513G>T