Canonical Allele Identifier: PA1139693629
Gene: SLC35A2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Ser241del
CA16043321
NM_001282651.2:c.721_723del