Canonical Allele Identifier: PA2828001356
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468
ClinVar RCV Id: RCV000220684 RCV002229315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala914Val
CA10578347
NM_001354902.2:c.2741C>T