Allele Registry

Canonical Allele Identifier: PA155209

Gene: SLC16A1 HGNC NCBI

ClinVar Allele:

135762

ClinVar RCV:

RCV000118353

RCV000399121

RCV001650964

RCV001807076

RCV001807077

ClinVar Variation:

130315

HGVS (amino-acid)	Matching Registered Transcripts
NP_003042.3:p.Asp490Glu	CA155208 NM_003051.4:c.1470T>A CA341826703 NM_003051.4:c.1470T>G