Canonical Allele Identifier: PA2825020694
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 993040
ClinVar RCV Id: RCV001283862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1535Ser
CA16031416
NM_000038.6:c.4604A>G