Canonical Allele Identifier: PA2825087373
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 898370
ClinVar RCV Id: RCV001142204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu310Arg
CA346740752
NM_000179.3:c.929T>G