Canonical Allele Identifier: PA2828004302
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2527Ser
CA16038396
NM_001354902.2:c.7580A>G