Canonical Allele Identifier: PA645419183
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 280619
ClinVar RCV Id: RCV000351397
ClinVar Variation Id: 372965
ClinVar RCV Id: RCV000414679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092.1:p.Trp340Cys
CA10602960
NM_001101.5:c.1020G>T
CA16042680
NM_001101.5:c.1020G>C