Canonical Allele Identifier: PA2825084978
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 825980
ClinVar RCV Id: RCV001862292 RCV001024550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp19Glu
CA346734562
NM_000179.3:c.57T>A
CA346734563
NM_000179.3:c.57T>G