Canonical Allele Identifier: PA2827989153
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 854549
ClinVar RCV Id: RCV003649358 RCV004031889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met2323Ile
CA16036777
NM_001354900.2:c.6969G>A
CA16036778
NM_001354900.2:c.6969G>C
CA16036779
NM_001354900.2:c.6969G>T