Canonical Allele Identifier: PA2827982432
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141276
ClinVar RCV Id: RCV000129720 RCV000211896 RCV000229223 RCV002478388 RCV003315881 RCV003997520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp226Gly
CA015607
NM_001354900.2:c.677A>G