Canonical Allele Identifier: PA2827988929
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2255Asn
CA16036358
NM_001354900.2:c.6764G>A