Canonical Allele Identifier: PA299519
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182660
ClinVar RCV Id: RCV000205769 RCV000491170 RCV000663327 RCV000587383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr750Lys
CA009894
NM_000179.3:c.2249C>A