Canonical Allele Identifier: PA891846976
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 565729
ClinVar RCV Id: RCV000685363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092.1:p.Thr229Met
CA366702096
NM_001101.5:c.686C>T