Canonical Allele Identifier: PA2827957649
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1128Ser
CA16028677
NM_001354897.2:c.3383A>G