Canonical Allele Identifier: PA16039994
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231898
ClinVar RCV Id: RCV000213972 RCV000348692 RCV004525836 RCV003650488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met1638Thr
CA040178
NM_000038.6:c.4913T>C