Canonical Allele Identifier: PA2825023969
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672
ClinVar RCV Id: RCV003653389 RCV002286789 RCV002363135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2369Leu
CA16036808
NM_000038.6:c.7106C>T