Canonical Allele Identifier: PA2827969700
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230821
ClinVar RCV Id: RCV004522935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1969Ala
CA16034424
NM_001354898.2:c.5906A>C