Canonical Allele Identifier: PA2827417880
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 96985
ClinVar RCV Id: RCV000083249
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334848.2:p.Ala281Val
CA224426
NM_001347919.2:c.842C>T