Canonical Allele Identifier: PA645469226
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 430221
ClinVar RCV Id: RCV000492861 RCV000634555
ClinVar Variation Id: 556774
ClinVar RCV Id: RCV000672826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Trp53Arg
CA373278633
NM_000155.4:c.157T>A
CA373278634
NM_000155.4:c.157T>C