Canonical Allele Identifier: PA2826636897
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89322
ClinVar RCV Id: RCV000218618 RCV000455514 RCV000629775 RCV002273954 RCV003460673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg674His
CA011105
NM_001281494.2:c.2021G>A