Canonical Allele Identifier: PA103769
Gene: HYLS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128265.1:p.Asp211Gly
CA114795
NM_001134793.2:c.632A>G