Canonical Allele Identifier: PA2580282824
Gene: SNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2321369
ClinVar RCV Id: RCV004166537
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003090.2:p.Val147Gly
CA392820503
NM_003099.4:c.440T>G