Canonical Allele Identifier: PA2827968569
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1625Ser
CA040262
NM_001354898.2:c.4874A>G