Canonical Allele Identifier: PA1139673822
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 942044
ClinVar RCV Id: RCV001211951 RCV002402627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser580Trp
CA346748831
NM_000179.3:c.1739C>G