Canonical Allele Identifier: PA185982
Gene: ALG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 183018
ClinVar RCV Id: RCV000161140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149078.1:p.Gly72_Leu75delinsSerProArg
CA185981
NM_033087.4:c.214_224delinsAGTCCCCG