Canonical Allele Identifier: PA2827988939
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411353
ClinVar RCV Id: RCV003766557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2258Ser
CA16036378
NM_001354900.2:c.6772C>T