Allele Registry

Canonical Allele Identifier: PA110294

Gene: SLC16A2 HGNC NCBI

ClinVar RCV:

RCV000012400

RCV000790835

ClinVar Variation:

11634

HGVS (amino-acid)	Matching Registered Transcripts
NP_006508.2:p.Ala150Val	CA222962 NM_006517.5:c.449C>T