Canonical Allele Identifier: PA915984661
Gene: GALT HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Phe85Leu
CA252849
NM_001258332.2:c.253T>C
CA373281899
NM_001258332.2:c.255C>A
CA373281903
NM_001258332.2:c.255C>G