Canonical Allele Identifier: PA2580282829
Gene: SNX1 HGNC NCBI
ClinVar RCV:
RCV004136235
ClinVar Variation:
2282889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003090.2:p.Pro271Thr
CA7607849
NM_003099.4:c.811C>A