Allele Registry

Canonical Allele Identifier: PA2826032950

Gene: HPSE HGNC NCBI

ClinVar RCV:

RCV003982087

ClinVar Variation:

3060058

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159970.1:p.Lys307Arg	CA2988977 NM_001166498.3:c.920A>G