Canonical Allele Identifier: PA2573163897
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477214
ClinVar RCV Id: RCV001998310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr914Ala
CA346755395
NM_000179.3:c.2740A>G