Allele Registry

Canonical Allele Identifier: PA119999

Gene: SLC16A1 HGNC NCBI

ClinVar RCV:

RCV000009470

RCV000193787

RCV002054429

ClinVar Variation:

8915

HGVS (amino-acid)	Matching Registered Transcripts
NP_003042.3:p.Gly472Arg	CA119998 NM_003051.4:c.1414G>A CA341826827 NM_003051.4:c.1414G>C