Canonical Allele Identifier: PA658679978
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483796
ClinVar RCV Id: RCV000561350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly31Cys
CA346734821
NM_000179.3:c.91G>T