Canonical Allele Identifier: PA645378395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 427607
ClinVar RCV Id: RCV001020758 RCV001249983 RCV001041513 RCV003492074 RCV003235247 RCV002475965 RCV004003433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg121His
CA071525
NM_000179.3:c.362G>A