Canonical Allele Identifier: PA2827959801
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219794
ClinVar RCV Id: RCV000575576 RCV003765323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1771Ser
CA041233
NM_001354897.2:c.5312A>G