Canonical Allele Identifier: PA2827962519
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His2601Pro
CA049129
NM_001354897.2:c.7802A>C