Canonical Allele Identifier: PA2827981908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41504
ClinVar RCV Id: RCV000034386 RCV000167102 RCV000410052 RCV003650354 RCV003996154 RCV003155048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser68Gly
CA008675
NM_001354900.2:c.202A>G