Canonical Allele Identifier: PA2827985112
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141041
ClinVar RCV Id: RCV000129376 RCV001775620 RCV003997497 RCV003764863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1097His
CA008365
NM_001354900.2:c.3289G>C