Canonical Allele Identifier: PA658744388
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491992
ClinVar RCV Id: RCV000584543 RCV000705703 RCV001174609 RCV004002357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile258Thr
CA346740217
NM_000179.3:c.773T>C