Canonical Allele Identifier: PA913199877
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 3616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Phe62Ser
CA340106
NM_001258332.2:c.185T>C