Canonical Allele Identifier: PA2827418172
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167206
ClinVar RCV Id: RCV004464571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334856.1:p.Arg138Met
CA6366576
NM_001347927.2:c.413G>T