Canonical Allele Identifier: PA2828002652
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1559Ser
CA040262
NM_001354902.2:c.4676A>G