Canonical Allele Identifier: PA2830290852
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_683758.1:p.Glu307Asp
CA7607935
NM_148955.4:c.921G>T
CA392824890
NM_148955.4:c.921G>C