Canonical Allele Identifier: PA2827977913
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231351
ClinVar RCV Id: RCV000239282 RCV003534516 RCV000213949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1677Ser
CA10578395
NM_001354899.2:c.5030C>G
CA16032509
NM_001354899.2:c.5029A>T