Canonical Allele Identifier: PA2827971894
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2001344
ClinVar RCV Id: RCV003742896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp2638Asn
CA16038677
NM_001354898.2:c.7912G>A