Canonical Allele Identifier: PA658689429
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_001120982.1:p.Asp2656Asn
CA16038630
NM_001127510.3:c.7966G>A