Canonical Allele Identifier: PA2828011666
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231149
ClinVar RCV Id: RCV004525220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2277Phe
CA046940
NM_001354902.2:c.6830C>T