Canonical Allele Identifier: PA2826629493
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 652505
ClinVar RCV Id: RCV001018798 RCV000808066 RCV001585735 RCV001779078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met1Leu