Canonical Allele Identifier: PA2827959085
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys1553Glu
CA10578378
NM_001354897.2:c.4657A>G