Canonical Allele Identifier: PA2825089351
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230528
ClinVar RCV Id: RCV004520679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn742Asp
CA346752456
NM_000179.3:c.2224A>G