Canonical Allele Identifier: PA295872
Gene: ACTC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005150.1:p.Phe257Leu
CA019904
NM_005159.5:c.769T>C
CA391629784
NM_005159.5:c.771C>G
CA391629786
NM_005159.5:c.771C>A