Canonical Allele Identifier: PA645379239
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 371790
ClinVar RCV Id: RCV000410264 RCV000576046 RCV001361344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser314Asn
CA073598
NM_000179.3:c.941G>A