Canonical Allele Identifier: PA916044382
Gene: PHKB HGNC NCBI

Linked Data

ClinVar Variation Id: 522767
ClinVar RCV Id: RCV000625928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350766.1:p.Thr68Ile
CA396098603
NM_001363837.1:c.203C>T