Canonical Allele Identifier: PA1139741846
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 862502
ClinVar RCV Id: RCV002554570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2591Phe
CA16038092
NM_001354896.2:c.7771A>T