Canonical Allele Identifier: PA2580139268
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 1703499
ClinVar RCV Id: RCV002280076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092.1:p.Ser60Arg
CA366706105
NM_001101.5:c.180C>G
CA366706109
NM_001101.5:c.180C>A
CA366706122
NM_001101.5:c.178A>C