Canonical Allele Identifier: PA149089
Gene: SHROOM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 95971
ClinVar RCV Id: RCV000082025 RCV001807030
ClinVar Variation Id: 287471
ClinVar RCV Id: RCV000322654 RCV002494870
ClinVar Variation Id: 590255
ClinVar RCV Id: RCV004026923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065768.2:p.Glu1151dup