Canonical Allele Identifier: PA330479
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89321
ClinVar RCV Id: RCV000552775 RCV003398659 RCV002433573 RCV004528271 RCV003477462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr969Ser
CA011072
NM_000179.3:c.2906A>C