Canonical Allele Identifier: PA2825087883
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 963892
ClinVar RCV Id: RCV001237996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala393Pro
CA346742352
NM_000179.3:c.1177G>C