Canonical Allele Identifier: PA2827962492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 953942
ClinVar RCV Id: RCV003650782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2593Asn
CA16038162
NM_001354897.2:c.7779A>C
CA16038163
NM_001354897.2:c.7779A>T