Canonical Allele Identifier: PA2827417853
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167206
ClinVar RCV Id: RCV004464571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334847.2:p.Arg858Met
CA6366576
NM_001347918.2:c.2573G>T