Canonical Allele Identifier: PA2827943037
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_001341824.1:p.Asp1138His
CA008365
NM_001354895.2:c.3412G>C