Canonical Allele Identifier: PA2827980857
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 859980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2572Glu
CA16038267
NM_001354899.2:c.7714C>G