Canonical Allele Identifier: PA2825304817
Gene: C1GALT1C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2053791
ClinVar RCV Id: RCV002922782 RCV004067012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011551.1:p.Asn202Lys
CA10505948
NM_001011551.3:c.606T>A
CA414207966
NM_001011551.3:c.606T>G