Canonical Allele Identifier: PA2827947802
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760417
ClinVar RCV Id: RCV002400793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Glu2582Asp
CA16038154
NM_001354895.2:c.7746A>C
CA16038155
NM_001354895.2:c.7746A>T