Canonical Allele Identifier: PA645383135
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233859
ClinVar RCV Id: RCV000219717 RCV000792117 RCV003463593 RCV003998583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu992Gly
CA10578124
NM_000179.3:c.2975A>G