Canonical Allele Identifier: PA2827989935
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629231
ClinVar RCV Id: RCV000773930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln2559His
CA16038272
NM_001354900.2:c.7677A>C
CA16038273
NM_001354900.2:c.7677A>T