Canonical Allele Identifier: PA2827957329
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1393312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1036Ser
CA16028071
NM_001354897.2:c.3107A>G