Canonical Allele Identifier: PA2827957323
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro1034Leu
CA16028060
NM_001354897.2:c.3101C>T