Canonical Allele Identifier: PA2580304918
Gene: CHST3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1914167
ClinVar RCV Id: RCV002590270

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004264.2:p.Pro176Leu
CA209479125
NM_004273.5:c.527C>T