Canonical Allele Identifier: PA658680404
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455360
ClinVar RCV Id: RCV000529561 RCV001180553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys324Gln
CA346740936
NM_000179.3:c.970A>C