Canonical Allele Identifier: PA2825092153
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 644095
ClinVar RCV Id: RCV000797936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1239Met
CA346761011
NM_000179.3:c.3717A>G