Canonical Allele Identifier: PA2828051789
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_001341834.1:p.Asp226Gly
CA015607
NM_001354905.2:c.677A>G