Allele Registry

Canonical Allele Identifier: PA2827164032

Gene: HPS1 HGNC NCBI

ClinVar RCV:

RCV002042388

RCV004526896

RCV004527060

ClinVar Variation:

1499624

3233780

HGVS (amino-acid)	Matching Registered Transcripts
NP_001309408.1:p.Leu635Pro	CA341630 NM_001322479.1:c.1904T>C CA2825001735 NM_001322479.1:c.1902_1904delinsCCC