Canonical Allele Identifier: PA207327
Gene: SHROOM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 212181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065768.2:p.Val1356Ile
CA207326
NM_020717.5:c.4066G>A