Canonical Allele Identifier: PA916056471
Gene: MSH5 HGNC NCBI

Linked Data

ClinVar Variation Id: 417969
ClinVar RCV Id: RCV000477966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079535.4:p.Asp504Tyr
CA16616947
NM_025259.6:c.1510G>T