Canonical Allele Identifier: PA2826505107
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_001254657.1:p.Cys198Ser
CA119265
NM_001267728.1:c.593G>C
CA388749679
NM_001267728.1:c.592T>A