Canonical Allele Identifier: PA2825092010
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396379
ClinVar RCV Id: RCV001902969 RCV003585148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1218Ser
CA071792
NM_000179.3:c.3652G>A