Canonical Allele Identifier: PA2827984714
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1315725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp975Tyr
CA16028002
NM_001354900.2:c.2923G>T