Canonical Allele Identifier: PA2825634856
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231149
ClinVar RCV Id: RCV004525220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2368Phe
CA046940
NM_001127510.3:c.7103C>T