Canonical Allele Identifier: PA2827550424
Gene: SNX14 HGNC NCBI

Linked Data

ClinVar Variation Id: 419155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337469.1:p.Asp867Ter
CA16618336
NM_001350540.2:c.2599_2605del