Canonical Allele Identifier: PA2826250724
Gene: SIAE HGNC NCBI
ClinVar RCV:
RCV003118418
ClinVar Variation:
2419893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186851.1:p.Cys414Ser
CA6341198
NM_001199922.2:c.1240T>A
CA383142226
NM_001199922.2:c.1241G>C