Canonical Allele Identifier: PA916041959
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193
ClinVar RCV Id: RCV000582096 RCV003653189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala459Val
CA16024253
NM_001354897.2:c.1376C>T