Canonical Allele Identifier: PA2827962349
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2550Ala
CA16037879
NM_001354897.2:c.7648C>G