Canonical Allele Identifier: PA131052
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 829
ClinVar RCV Id: RCV000000872 RCV000034389 RCV000035073 RCV000322880 RCV000579405 RCV001353725 RCV002286387 RCV003650352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu1317Gln
CA008815
NM_000038.6:c.3949G>C