Canonical Allele Identifier: PA2826313294
Gene: SNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167124
ClinVar RCV Id: RCV004464489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229862.1:p.Glu372Asp
CA7607935
NM_001242933.2:c.1116G>T
CA392824890
NM_001242933.2:c.1116G>C