Canonical Allele Identifier: PA143746
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50365
ClinVar RCV Id: RCV000043516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005651.1:p.Met1Ile
CA143744
NM_005660.3:c.3G>A
CA412899007
NM_005660.3:c.3G>T
CA412899009
NM_005660.3:c.3G>C