Canonical Allele Identifier: PA2580531721
Gene: SIAE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733746.1:p.Val431Met
CA6341239
NM_170601.5:c.1291G>A