Canonical Allele Identifier: PA2825021476
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745920
ClinVar RCV Id: RCV002338512

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1731Ser
CA16032678
NM_000038.6:c.5191G>T