Canonical Allele Identifier: PA913200300
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629228
ClinVar RCV Id: RCV000773927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly1721Val
CA16032616
NM_001127510.3:c.5162G>T