Canonical Allele Identifier: PA2826313290
Gene: SNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167129
ClinVar RCV Id: RCV004464494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229862.1:p.Leu313Val
CA7607896
NM_001242933.2:c.937C>G