Canonical Allele Identifier: PA2827962559
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_001341826.1:p.Asn2614Lys
CA10578451
NM_001354897.2:c.7842C>G
CA16038303
NM_001354897.2:c.7842C>A