Canonical Allele Identifier: PA2827947606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1040272
ClinVar RCV Id: RCV003652188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2522Ala
CA16037772
NM_001354895.2:c.7564C>G