Canonical Allele Identifier: PA2827989182
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757245
ClinVar RCV Id: RCV002367425 RCV003154250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met2332Ile
CA16036834
NM_001354900.2:c.6996G>A
CA16036835
NM_001354900.2:c.6996G>C
CA16036836
NM_001354900.2:c.6996G>T