ClinGen Allele Registry
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Canonical Allele Identifier:
PA163181
Gene: HSD17B4
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000125465
RCV001092766
RCV001810425
RCV003764860
ClinVar Variation:
137616
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000405.1:p.Ala34Val
CA163180
NM_000414.4:c.101C>T