Canonical Allele Identifier: PA2826313280
Gene: SNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2539176
ClinVar RCV Id: RCV004311523
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229862.1:p.Val94Met
CA7607656
NM_001242933.2:c.280G>A