Canonical Allele Identifier: PA2828000301
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2777735
ClinVar RCV Id: RCV003745645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala358Gly
CA16024252
NM_001354902.2:c.1073C>G