Canonical Allele Identifier: PA195116
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186538
ClinVar RCV Id: RCV000166149 RCV000456613 RCV001775649 RCV003462201 RCV003995483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg901Cys
CA010754
NM_000179.3:c.2701C>T