Canonical Allele Identifier: PA2825025139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg2670Ile
CA16038731
NM_000038.6:c.8009G>T