Canonical Allele Identifier: PA2828009472
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1606Ala
CA10578392
NM_001354902.2:c.4816A>G