Canonical Allele Identifier: PA2830246046
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 127896
ClinVar RCV Id: RCV000115822 RCV000233793 RCV000709427 RCV000656967 RCV001354391 RCV001818279 RCV003149804 RCV003492497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598332.1:p.Ile199Asn
CA287993
NM_133629.3:c.596T>A