Canonical Allele Identifier: PA2827968917
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 864178
ClinVar RCV Id: RCV003650594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1731Ala
CA16032845
NM_001354898.2:c.5191T>G
CA916079919
NM_001354898.2:c.5190_5193delinsTGCG