Allele Registry

Canonical Allele Identifier: PA108512

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV001924022

ClinVar Variation:

1424767

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Val446Phe	CA342676 NM_003060.4:c.1336G>T