Canonical Allele Identifier: PA2826313277
Gene: SNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2364689
ClinVar RCV Id: RCV004201972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229862.1:p.Thr48Ala
CA7607594
NM_001242933.2:c.142A>G