Canonical Allele Identifier: PA2828004187
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1170969
ClinVar RCV Id: RCV001523852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2451Asp
CA16037890
NM_001354902.2:c.7351A>G