Canonical Allele Identifier: PA2826635078
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234200
ClinVar RCV Id: RCV000215555 RCV000463760 RCV001753682 RCV003998606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His250Gln
CA067967
NM_001281494.2:c.750T>A
CA346747303
NM_001281494.2:c.750T>G