Canonical Allele Identifier: PA645462285
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 229719
ClinVar RCV Id: RCV000216942 RCV000534748 RCV001560841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Ser207Pro
CA10580452
NM_002878.4:c.619T>C