Allele Registry

Canonical Allele Identifier: PA263931

Gene: SLC17A5 HGNC NCBI

ClinVar RCV:

RCV000005973

RCV000049971

RCV000485185

ClinVar Variation:

56558

HGVS (amino-acid)	Matching Registered Transcripts
NP_036566.1:p.Ser268_Asn272del	CA263930 NM_012434.5:c.802_816del