Canonical Allele Identifier: PA658660735
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470099
ClinVar RCV Id: RCV002395425 RCV003742790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2529Val
CA16037818
NM_001127510.3:c.7586C>T