Canonical Allele Identifier: PA2825025080
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433679
ClinVar RCV Id: RCV000502714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp2656Tyr
CA16038632
NM_000038.6:c.7966G>T