Canonical Allele Identifier: PA111199
Gene: ACTG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186883.1:p.Ala135Val
CA219948
NM_001199954.3:c.404C>T