Canonical Allele Identifier: PA2827961645
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_001341826.1:p.Pro2334Ser
CA046567
NM_001354897.2:c.7000C>T