Canonical Allele Identifier: PA204922
Gene: ACTG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208792
ClinVar RCV Id: RCV000190820 RCV000210360 RCV001376053 RCV001574649 RCV001535812
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001606.1:p.Arg257His
CA204921
NM_001615.4:c.770G>A