Allele Registry

Canonical Allele Identifier: PA2828440065

Gene: SLC16A11 HGNC NCBI

ClinVar RCV:

RCV001540485

ClinVar Variation:

1182780

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357478.1:p.Asp103Gly	CA8335325 NM_001370549.1:c.308A>G