Canonical Allele Identifier: PA2827989785
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His2513Tyr
CA16037974
NM_001354900.2:c.7537C>T