Canonical Allele Identifier: PA891858703
Gene: SHROOM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 590244
ClinVar RCV Id: RCV000721070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065768.2:p.Tyr170Cys
CA10416350
NM_020717.5:c.509A>G