Canonical Allele Identifier: PA645381719
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410422
ClinVar RCV Id: RCV002429525 RCV002230106 RCV004001825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn742Ser
CA16611000
NM_000179.3:c.2225A>G