Canonical Allele Identifier: PA1139732434
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His402Tyr
CA16023877
NM_001354897.2:c.1204C>T