Canonical Allele Identifier: PA2827962182
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2500Val
CA048153
NM_001354897.2:c.7499A>T