Canonical Allele Identifier: PA2825021207
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 651065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1665Ala
CA16032259
NM_000038.6:c.4993C>G