Canonical Allele Identifier: PA2828009488
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1614Ser
CA10578395
NM_001354902.2:c.4841C>G
CA16032509
NM_001354902.2:c.4840A>T