Canonical Allele Identifier: PA2828011468
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1417078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro2233Ser
CA046567
NM_001354902.2:c.6697C>T