Canonical Allele Identifier: PA2825024756
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827223
ClinVar RCV Id: RCV001026757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2576Ser
CA16038110
NM_000038.6:c.7726G>T