Canonical Allele Identifier: PA2828003133
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1812Ser
CA042707
NM_001354902.2:c.5435A>G