Canonical Allele Identifier: PA2828027593
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2086Leu
CA16036808
NM_001354906.2:c.6257C>T