Canonical Allele Identifier: PA2827994199
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Tyr1084Cys
CA16028846
NM_001354901.2:c.3251A>G