Canonical Allele Identifier: PA645469764
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 281044
ClinVar RCV Id: RCV000386913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Arg228Thr
CA10603791
NM_000155.4:c.683G>C