Canonical Allele Identifier: PA2573205652
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1417078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2342Ser
CA046567
NM_001354896.2:c.7024C>T