Canonical Allele Identifier: PA2827989667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156483
ClinVar RCV Id: RCV000144574 RCV000572226 RCV000759443 RCV003534393 RCV003492634 RCV003998160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Tyr2476Cys
CA013809
NM_001354900.2:c.7427A>G