Canonical Allele Identifier: PA2827962108
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2478Pro
CA013665
NM_001354897.2:c.7432T>C