Canonical Allele Identifier: PA2827970911
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_001341827.1:p.Ser2343Phe
CA046940
NM_001354898.2:c.7028C>T