Canonical Allele Identifier: PA2825024960
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1052468
ClinVar RCV Id: RCV003771065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2627Ala
CA16038452
NM_000038.6:c.7879T>G