Canonical Allele Identifier: PA2825085047
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2490563
ClinVar RCV Id: RCV003215392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu30Asp
CA346734817
NM_000179.3:c.90A>C
CA346734818
NM_000179.3:c.90A>T