Canonical Allele Identifier: PA2827949383
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220329
ClinVar RCV Id: RCV000204305 RCV000564542 RCV002228948 RCV003153486 RCV003997632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala239Pro
CA047113
NM_001354896.2:c.715G>C