Canonical Allele Identifier: PA2827959477
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1677Asp
CA040350
NM_001354897.2:c.5029A>G