Canonical Allele Identifier: PA2828004126
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2419Ser
CA10578446
NM_001354902.2:c.7256A>G