Canonical Allele Identifier: PA2827976034
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1731187
ClinVar RCV Id: RCV002332997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp1110Tyr
CA16028813
NM_001354899.2:c.3328G>T