Canonical Allele Identifier: PA2827948049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659988
ClinVar RCV Id: RCV001027009 RCV003653392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp2656Glu
CA16038636
NM_001354895.2:c.7968T>A
CA16038637
NM_001354895.2:c.7968T>G