Canonical Allele Identifier: PA2829784325
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167206
ClinVar RCV Id: RCV004464571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055573.3:p.Arg898Met
CA6366576
NM_014758.3:c.2693G>T