Canonical Allele Identifier: PA238872
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 193347
ClinVar RCV Id: RCV000173412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Ala106Pro
CA238871
NM_006517.5:c.316G>C