Canonical Allele Identifier: PA194987
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186492
ClinVar RCV Id: RCV000166094 RCV000206584 RCV000524150 RCV000662779 RCV000759855 RCV001375566 RCV003462200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn984His
CA011176
NM_000179.3:c.2950A>C