Canonical Allele Identifier: PA2827970779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1417078
ClinVar RCV Id: RCV001936032 RCV004043558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2299Ser
CA046567
NM_001354898.2:c.6895C>T