Canonical Allele Identifier: PA2826250706
Gene: SIAE HGNC NCBI
ClinVar RCV:
RCV003844474
ClinVar Variation:
2988291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186851.1:p.Ala381Val
CA383144273
NM_001199922.2:c.1142C>T