Canonical Allele Identifier: PA2828023208
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_001341835.1:p.Thr1422Ser
CA10578395
NM_001354906.2:c.4265C>G
CA16032509
NM_001354906.2:c.4264A>T