Canonical Allele Identifier: PA2826250713
Gene: SIAE HGNC NCBI
ClinVar RCV:
RCV002627191
ClinVar Variation:
1933753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186851.1:p.Val396Met
CA6341239
NM_001199922.2:c.1186G>A