Allele Registry

Canonical Allele Identifier: PA110350

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000020651

ClinVar Variation:

21463

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Ser120Phe	CA342116 NM_006517.5:c.359C>T