Canonical Allele Identifier: PA2827970898
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127317
ClinVar RCV Id: RCV000115119 RCV001026018 RCV003534344 RCV003997229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys2338Arg
CA012825
NM_001354898.2:c.7013A>G