Canonical Allele Identifier: PA2826313285
Gene: SNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2292461
ClinVar RCV Id: RCV004144293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229862.1:p.Phe206Tyr
CA392822423
NM_001242933.2:c.617T>A