Canonical Allele Identifier: PA2825020692
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587035
ClinVar RCV Id: RCV003339112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1535His
CA16031412
NM_000038.6:c.4603A>C