Canonical Allele Identifier: PA2827979628
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127314
ClinVar RCV Id: RCV000115113 RCV000573892 RCV003534343 RCV003997228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2203Phe
CA012398
NM_001354899.2:c.6607A>T