ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828525538
Gene: HSD17B4
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000023152
RCV002513181
RCV003330398
ClinVar Variation:
30228
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001361429.1:p.Tyr70Cys
CA129040
NM_001374500.1:c.209A>G