Canonical Allele Identifier: PA2827971320
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp2465Val
CA048153
NM_001354898.2:c.7394A>T