Canonical Allele Identifier: PA2827963540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Tyr71Cys
CA033841
NM_001354898.2:c.212A>G