Canonical Allele Identifier: PA2827997060
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Tyr1948His
CA043743
NM_001354901.2:c.5842T>C