Canonical Allele Identifier: PA287270
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89218
ClinVar RCV Id: RCV000115381 RCV000524118 RCV000409690 RCV000491847 RCV003235029 RCV003997068 RCV003466935 RCV003993789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg577Cys
CA009088
NM_000179.3:c.1729C>T