Canonical Allele Identifier: PA2827974717
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188223
ClinVar RCV Id: RCV000218100 RCV000484713 RCV002291585 RCV003995610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser719Leu
CA007315
NM_001354899.2:c.2156C>T