Canonical Allele Identifier: PA2827981953
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41529
ClinVar RCV Id: RCV000034414 RCV000409727 RCV000579781 RCV003534320 RCV003996163 RCV003317056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu81Asp
CA008951
NM_001354900.2:c.243G>C
CA16022242
NM_001354900.2:c.243G>T