Canonical Allele Identifier: PA2827977488
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp1542Glu
CA10578381
NM_001354899.2:c.4626T>A
CA16031660
NM_001354899.2:c.4626T>G