Canonical Allele Identifier: PA2827989707
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411449
ClinVar RCV Id: RCV000567469 RCV003766578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2490Ala
CA16037824
NM_001354900.2:c.7468T>G