Canonical Allele Identifier: PA2827959777
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1765Val
CA041104
NM_001354897.2:c.5294C>T