Canonical Allele Identifier: PA2827465221
Gene: HPS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336827.1:p.Pro624Leu
CA10163175
NM_001349898.2:c.1871C>T