Canonical Allele Identifier: PA2827417850
Gene: SNX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2225582
ClinVar RCV Id: RCV004084803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334847.2:p.Gly847Asp
CA383457782
NM_001347918.2:c.2540G>A