Allele Registry

Canonical Allele Identifier: PA092729

Gene: GALT HGNC NCBI

ClinVar RCV:

RCV000022041

ClinVar Variation:

25115

HGVS (amino-acid)	Matching Registered Transcripts
NP_000146.2:p.Gln9His	CA259311 NM_000155.4:c.27G>C CA373278237 NM_000155.4:c.27G>T