Canonical Allele Identifier: PA2827962422
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val2571Ile
CA16038011
NM_001354897.2:c.7711G>A