Canonical Allele Identifier: PA2827982933
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1770136
ClinVar RCV Id: RCV002387484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His385Tyr
CA16024219
NM_001354900.2:c.1153C>T