Canonical Allele Identifier: PA916041158
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133520
ClinVar RCV Id: RCV000120027 RCV003764835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2270Ala
CA012481
NM_001354896.2:c.6808C>G