Canonical Allele Identifier: PA2826250734
Gene: SIAE HGNC NCBI

Linked Data

ClinVar Variation Id: 1485806
ClinVar RCV Id: RCV002001009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186851.1:p.Gln427Arg
CA6341186
NM_001199922.2:c.1280A>G