Canonical Allele Identifier: PA156788
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_001120982.1:p.Pro2252Ala
CA012481
NM_001127510.3:c.6754C>G