This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2825867785
Gene: DST HGNC NCBI
ClinVar RCV:
RCV004018424
ClinVar Variation:
3076107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138242.1:p.Asn2973Lys
CA364516422
NM_001144770.2:c.8919T>G
CA364516423
NM_001144770.2:c.8919T>A