Canonical Allele Identifier: PA2827983504
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser593Arg
CA10578330
NM_001354900.2:c.1779T>G
CA16025473
NM_001354900.2:c.1777A>C
CA16025479
NM_001354900.2:c.1779T>A