Canonical Allele Identifier: PA2828011358
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231142
ClinVar RCV Id: RCV004525213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2191Ser
CA16036697
NM_001354905.2:c.6571C>T