Canonical Allele Identifier: PA1139741871
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927906
ClinVar RCV Id: RCV001191479 RCV004010515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys2608Asn
CA16038210
NM_001354896.2:c.7824A>C
CA16038211
NM_001354896.2:c.7824A>T