Canonical Allele Identifier: PA2828004608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2719Ser
CA015484
NM_001354902.2:c.8156A>G