Canonical Allele Identifier: PA131032
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41519
ClinVar RCV Id: RCV000034404 RCV000035065 RCV000144567 RCV000159535 RCV003904891 RCV004018732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser535Phe
CA005357
NM_000038.6:c.1604C>T