Canonical Allele Identifier: PA2830290838
Gene: SNX1 HGNC NCBI
ClinVar RCV:
RCV004144293
ClinVar Variation:
2292461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683758.1:p.Phe141Tyr
CA392822423
NM_148955.4:c.422T>A