Canonical Allele Identifier: PA1139741513
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 857579
ClinVar RCV Id: RCV003649364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Met2391Lys
CA16036831
NM_001354896.2:c.7172T>A