Canonical Allele Identifier: PA2825024786
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760417
ClinVar RCV Id: RCV002400793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu2582Asp
CA16038154
NM_000038.6:c.7746A>C
CA16038155
NM_000038.6:c.7746A>T