Canonical Allele Identifier: PA2827963964
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln198His
CA012417
NM_001354898.2:c.594A>C
CA16022798
NM_001354898.2:c.594A>T