Canonical Allele Identifier: PA2826636949
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234538
ClinVar RCV Id: RCV000214813 RCV000534216 RCV000566696 RCV001354499 RCV003998623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg686His
CA069876
NM_001281494.2:c.2057G>A