Canonical Allele Identifier: PA176317
Gene: HPS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 163673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071364.4:p.Leu443Val
CA176313
NM_022081.5:c.1327C>G