Canonical Allele Identifier: PA2827471922
Gene: HPS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1903642
ClinVar RCV Id: RCV002573075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336834.1:p.Ala645Ser
CA10163151
NM_001349905.1:c.1933G>T