Canonical Allele Identifier: PA2827961773
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231149
ClinVar RCV Id: RCV004525220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2378Phe
CA046940
NM_001354897.2:c.7133C>T