Canonical Allele Identifier: PA2827997608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470052
ClinVar RCV Id: RCV000573529 RCV001569317 RCV003999415 RCV003409800 RCV002526312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2126Asn
CA045325
NM_001354901.2:c.6377G>A