Canonical Allele Identifier: PA658679972
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485850
ClinVar RCV Id: RCV000568043 RCV000796511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg29Cys
CA346734808
NM_000179.3:c.85C>T