Canonical Allele Identifier: PA299449
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182630
ClinVar RCV Id: RCV000160675 RCV000214441 RCV000233389 RCV000662835 RCV003998495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp667His
CA009534
NM_000179.3:c.1999G>C