Allele Registry

Canonical Allele Identifier: PA261026

Gene: GALT HGNC NCBI

ClinVar RCV:

RCV000031852

ClinVar Variation:

37355

HGVS (amino-acid)	Matching Registered Transcripts
NP_000146.2:p.Asp28Asn	CA261025 NM_000155.4:c.82G>A