Canonical Allele Identifier: PA295848
Gene: ACTG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180620
ClinVar RCV Id: RCV000157596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001606.1:p.Arg148Leu
CA295847
NM_001615.4:c.443G>T