Canonical Allele Identifier: PA2827418110
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167206
ClinVar RCV Id: RCV004464571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334853.1:p.Arg238Met
CA6366576
NM_001347924.2:c.713G>T