ClinGen Allele Registry
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Canonical Allele Identifier:
PA915979694
Gene: RAD51D
HGNC
NCBI
Linked Data
ClinVar Variation Id:
127896
ClinVar RCV Id:
RCV000115822
RCV000233793
RCV000709427
RCV000656967
RCV001354391
RCV001818279
RCV003149804
RCV003492497
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001136043.1:p.Ile331Asn
CA287993
NM_001142571.2:c.992T>A