Canonical Allele Identifier: PA2825091468
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023941
ClinVar RCV Id: RCV001324060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1150Val
CA346759960
NM_000179.3:c.3448T>G