Canonical Allele Identifier: PA2827989570
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp2449Val
CA048153
NM_001354900.2:c.7346A>T