Canonical Allele Identifier: PA2827963350
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2852Ala
CA015593
NM_001354897.2:c.8554T>G