Canonical Allele Identifier: PA2828002432
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1742135
ClinVar RCV Id: RCV002330441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1457Lys
CA16031507
NM_001354902.2:c.4371C>A
CA16031508
NM_001354902.2:c.4371C>G