Canonical Allele Identifier: PA645448797
Gene: SHROOM3 HGNC NCBI

Linked Data

ClinVar Variation Id: 403438
ClinVar RCV Id: RCV000455435 RCV003972740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065910.3:p.Ser325Ala
CA2972268
NM_020859.4:c.973T>G