Canonical Allele Identifier: PA2827965244
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser609Arg
CA10578330
NM_001354898.2:c.1827T>G
CA16025473
NM_001354898.2:c.1825A>C
CA16025479
NM_001354898.2:c.1827T>A