Canonical Allele Identifier: PA2828015004
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_001341835.1:p.Asp113Glu
CA16023905
NM_001354906.2:c.339T>A
CA16023906
NM_001354906.2:c.339T>G