Canonical Allele Identifier: PA2573088726
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1338485
ClinVar RCV Id: RCV001817856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Trp109Arg
CA413656243
NM_006517.5:c.325T>A
CA413656244
NM_006517.5:c.325T>C