Canonical Allele Identifier: PA645384985
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410463
ClinVar RCV Id: RCV000463911 RCV000485411 RCV000566983 RCV000662834 RCV003463934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His1317Asp
CA072360
NM_000179.3:c.3949C>G