Canonical Allele Identifier: PA250779
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82636
ClinVar RCV Id: RCV000073625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met2713Leu
CA014373
NM_000038.6:c.8137A>C
CA16039003
NM_000038.6:c.8137A>T