Canonical Allele Identifier: PA2828027755
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231149
ClinVar RCV Id: RCV004525220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2267Phe
CA046940
NM_001354903.2:c.6800C>T