Canonical Allele Identifier: PA2825639622
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_001120983.2:p.Gly956Asp
CA16027713
NM_001127511.3:c.2867G>A