Canonical Allele Identifier: PA111567
Gene: GK HGNC NCBI

Linked Data

ClinVar Variation Id: 10946
ClinVar RCV Id: RCV000011693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191948.1:p.Trp509Arg
CA121272
NM_001205019.2:c.1525T>C
CA412642345
NM_001205019.2:c.1525T>A