Canonical Allele Identifier: PA2827464546
Gene: HPS4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336827.1:p.His154Arg
CA342358
NM_001349898.2:c.461A>G