Canonical Allele Identifier: PA2827973419
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1414515
ClinVar RCV Id: RCV003772806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly281Ala
CA16023336
NM_001354899.2:c.842G>C