Canonical Allele Identifier: PA213206
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 127161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092.1:p.Leu65Phe
CA213204
NM_001101.5:c.193C>T