Canonical Allele Identifier: PA2827960608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Tyr2017His
CA043743
NM_001354897.2:c.6049T>C