Canonical Allele Identifier: PA2827999397
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140954
ClinVar RCV Id: RCV000129235 RCV000206635 RCV002228307 RCV003148656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val2657Met
CA014393
NM_001354901.2:c.7969G>A