Canonical Allele Identifier: PA658680781
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479893
ClinVar RCV Id: RCV000563700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile651Val
CA068307
NM_000179.3:c.1951A>G