Canonical Allele Identifier: PA2828011360
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2205Asn
CA16036358
NM_001354902.2:c.6614G>A