Canonical Allele Identifier: PA2827247698
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 516978
ClinVar RCV Id: RCV000616315 RCV001033980 RCV002314171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311221.1:p.Phe5Leu
CA10493417
NM_001324292.2:c.13T>C
CA414247972
NM_001324292.2:c.15T>A
CA414247973
NM_001324292.2:c.15T>G