Canonical Allele Identifier: PA338667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216181
ClinVar RCV Id: RCV000775352 RCV003765284 RCV003996980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn2618Asp
CA338662
NM_001127510.3:c.7852A>G