Canonical Allele Identifier: PA2499229341
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1047296
ClinVar RCV Id: RCV001351990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His785Leu
CA346753554
NM_000179.3:c.2354A>T