Canonical Allele Identifier: PA658671957
Gene: SNX27 HGNC NCBI

Linked Data

ClinVar Variation Id: 462808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112180.4:p.Val442Ile
CA1093642
NM_030918.6:c.1324G>A