Canonical Allele Identifier: PA2825087590
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011661
ClinVar RCV Id: RCV001309496 RCV002322216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu337Ser
CA346741252
NM_000179.3:c.1010T>C