Canonical Allele Identifier: PA2826661665
Gene: SLC35A2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269577.1:p.Cys58Phe
CA412897640
NM_001282648.2:c.173G>T