Allele Registry

Canonical Allele Identifier: PA2826707774

Gene: SLC17A4 HGNC NCBI

ClinVar RCV:

RCV001609662

ClinVar Variation:

1229422

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273050.1:p.Ala318Thr	CA3662275 NM_001286121.1:c.952G>A