Canonical Allele Identifier: PA2827996094
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1657Ser
CA040767
NM_001354901.2:c.4970A>G