Canonical Allele Identifier: PA2827983784
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Tyr696His
CA031174
NM_001354900.2:c.2086T>C