Canonical Allele Identifier: PA2827985038
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1077Ser
CA16028677
NM_001354900.2:c.3230A>G