Canonical Allele Identifier: PA2828011992
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371793
ClinVar RCV Id: RCV000410564 RCV001026397 RCV003535693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2377Ala
CA047997
NM_001354902.2:c.7129T>G