Canonical Allele Identifier: PA658801975
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525626
ClinVar RCV Id: RCV000629745 RCV004025370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro293Leu
CA346740664
NM_000179.3:c.878C>T