Canonical Allele Identifier: PA2827970680
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2271Asn
CA16036358
NM_001354898.2:c.6812G>A