Canonical Allele Identifier: PA916041644
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489501
ClinVar RCV Id: RCV000580553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2674Asn
CA16038630
NM_001354896.2:c.8020G>A