Canonical Allele Identifier: PA2827949823
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2848588
ClinVar RCV Id: RCV003744521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp396Glu
CA16023905
NM_001354896.2:c.1188T>A
CA16023906
NM_001354896.2:c.1188T>G