Canonical Allele Identifier: PA2741984921
Gene: ALG12 HGNC NCBI

Linked Data

ClinVar Variation Id: 3061429
ClinVar RCV Id: RCV003983437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077010.1:p.Ser36Arg
CA412081111
NM_024105.4:c.108C>G
CA412081114
NM_024105.4:c.108C>A
CA412081123
NM_024105.4:c.106A>C