Canonical Allele Identifier: PA645382021
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410525
ClinVar RCV Id: RCV000566667 RCV000464632 RCV000759132 RCV004001857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His785Gln
CA16611005
NM_000179.3:c.2355T>A
CA346753563
NM_000179.3:c.2355T>G