Canonical Allele Identifier: PA2827962516
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946681
ClinVar RCV Id: RCV003538615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His2601Arg
CA16038215
NM_001354897.2:c.7802A>G