Canonical Allele Identifier: PA272491
Gene: SLC16A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 159902
ClinVar RCV Id: RCV000147494 RCV000224827 RCV000624288 RCV001226584 RCV001847780
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006508.2:p.Arg371Cys
CA272490
NM_006517.5:c.1111C>T