Canonical Allele Identifier: PA658677083
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 478822
ClinVar RCV Id: RCV000550153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Asp302His
CA377147897
NM_004273.5:c.904G>C