Canonical Allele Identifier: PA323448
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 213744
ClinVar RCV Id: RCV000198918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Ser43Arg
CA323447
NM_030777.4:c.129C>G
CA409266393
NM_030777.4:c.127A>C
CA409266399
NM_030777.4:c.129C>A