Canonical Allele Identifier: PA2827947779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827223
ClinVar RCV Id: RCV001026757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala2576Ser
CA16038110
NM_001354895.2:c.7726G>T