Canonical Allele Identifier: PA658660318
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038
ClinVar RCV Id: RCV001190911 RCV003742758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2086Ala
CA044235
NM_001127510.3:c.6256C>G