Canonical Allele Identifier: PA2827980490
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2462Val
CA048153
NM_001354899.2:c.7385A>T