Canonical Allele Identifier: PA2828011245
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 826775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2178Ser
CA046630
NM_001354905.2:c.6532C>T