Canonical Allele Identifier: PA2828012363
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 647268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2489Phe
CA16038139
NM_001354902.2:c.7466C>T