Canonical Allele Identifier: PA2825629399
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2058749
ClinVar RCV Id: RCV003744821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly974Asp
CA16027713
NM_001127510.3:c.2921G>A