Canonical Allele Identifier: PA2825068032
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2683038
ClinVar RCV Id: RCV003481905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Asn173Lys
CA373281392
NM_000155.4:c.519C>A
CA373281395
NM_000155.4:c.519C>G