Canonical Allele Identifier: PA2829412542
Gene: SNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167124
ClinVar RCV Id: RCV004464489
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003090.2:p.Glu372Asp
CA7607935
NM_003099.4:c.1116G>T
CA392824890
NM_003099.4:c.1116G>C