Canonical Allele Identifier: PA2825644695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu2601Ala
CA10578452
NM_001127511.3:c.7802A>C