Canonical Allele Identifier: PA645381205
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237148
ClinVar RCV Id: RCV000229693 RCV000482874 RCV000491214 RCV001192456 RCV001356893 RCV001798729 RCV003469131 RCV003998712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys646Arg
CA068286
NM_000179.3:c.1937A>G