Canonical Allele Identifier: PA1139741718
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2508Val
CA048153
NM_001354896.2:c.7523A>T