Canonical Allele Identifier: PA1139677966
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 861344
ClinVar RCV Id: RCV002240544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp997His
CA16027993
NM_001127511.3:c.2989G>C