Canonical Allele Identifier: PA913191940
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 593279
ClinVar RCV Id: RCV000728274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Asn97Lys
CA373279246
NM_000155.4:c.291C>A
CA373279247
NM_000155.4:c.291C>G