Canonical Allele Identifier: PA2827417945
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 96985
ClinVar RCV Id: RCV000083249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334849.2:p.Ala281Val
CA224426
NM_001347920.2:c.842C>T