Canonical Allele Identifier: PA2826892309
Gene: SNX14 HGNC NCBI

Linked Data

ClinVar Variation Id: 419155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291408.1:p.Asp870Ter
CA16618336
NM_001304479.2:c.2608_2614del