Canonical Allele Identifier: PA2825644701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2765432
ClinVar RCV Id: RCV003538114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2604Ser
CA16038421
NM_001127511.3:c.7810C>T