Canonical Allele Identifier: PA2825024757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 918607
ClinVar RCV Id: RCV001176273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2576Pro
CA16038109
NM_000038.6:c.7726G>C