ClinGen Allele Registry
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Canonical Allele Identifier:
PA136917
Gene: WHRN
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000038892
RCV000334982
RCV000391015
RCV001095334
RCV001514504
ClinVar Variation:
45674
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_056219.3:p.Asn796Lys
CA136916
NM_015404.4:c.2388C>A
CA5205652
NM_015404.4:c.2388C>G