Canonical Allele Identifier: PA2827418088
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167206
ClinVar RCV Id: RCV004464571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334852.2:p.Arg323Met
CA6366576
NM_001347923.2:c.968G>T