Canonical Allele Identifier: PA915964628
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820355
ClinVar RCV Id: RCV001013728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile651Leu
CA346750538
NM_000179.3:c.1951A>C