Canonical Allele Identifier: PA916039669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 421285
ClinVar RCV Id: RCV000478621 RCV000491486 RCV003535757 RCV002525866 RCV004003349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr644Ala
CA029787
NM_001354896.2:c.1930A>G