Canonical Allele Identifier: PA114796
Gene: HYLS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659451.1:p.Asp211Gly
CA114795
NM_145014.3:c.632A>G