Canonical Allele Identifier: PA2827957292
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1026Val
CA16028005
NM_001354897.2:c.3077A>T