Canonical Allele Identifier: PA2827982758
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.His333Tyr
CA16023877
NM_001354900.2:c.997C>T