Canonical Allele Identifier: PA2827986486
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452745
ClinVar RCV Id: RCV003177519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1505Lys
CA16031493
NM_001354900.2:c.4515T>A
CA16031494
NM_001354900.2:c.4515T>G