Canonical Allele Identifier: PA2825024795
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2584Ser
CA16038165
NM_000038.6:c.7750G>T