Canonical Allele Identifier: PA645505395
Gene: MSH5 HGNC NCBI
ClinVar RCV:
RCV000477966
ClinVar Variation:
417969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_751897.1:p.Asp487Tyr
CA16616947
NM_172165.4:c.1459G>T