Canonical Allele Identifier: PA2827962608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760927
ClinVar RCV Id: RCV002412240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2631Tyr
CA16038417
NM_001354897.2:c.7892C>A