Canonical Allele Identifier: PA2825067941
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 280967
ClinVar RCV Id: RCV000333580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Ala78Thr
CA10603761
NM_000155.4:c.232G>A