Canonical Allele Identifier: PA916041578
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232691
ClinVar RCV Id: RCV000213566 RCV003650499 RCV003997996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2622Lys
CA10578451
NM_001354896.2:c.7866C>G
CA16038303
NM_001354896.2:c.7866C>A