Canonical Allele Identifier: PA2580131962
Gene: PAPSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2140719
ClinVar RCV Id: RCV003056593
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015880.1:p.Arg346Cys
CA5589628
NM_001015880.2:c.1036C>T