Canonical Allele Identifier: PA2826863483
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167206
ClinVar RCV Id: RCV004464571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288018.1:p.Arg278Met
CA6366576
NM_001301089.2:c.833G>T