Canonical Allele Identifier: PA2830434840
Gene: ING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8067
ClinVar RCV Id: RCV000008533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937861.1:p.Cys146Ser
CA119265
NM_198218.3:c.437G>C
CA388749679
NM_198218.3:c.436T>A