Canonical Allele Identifier: PA2827989783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231405
ClinVar RCV Id: RCV004525476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His2513Gln
CA16037978
NM_001354900.2:c.7539T>A
CA16037979
NM_001354900.2:c.7539T>G