Canonical Allele Identifier: PA891846190
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 584619
ClinVar RCV Id: RCV000708876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn827Thr
CA346754165
NM_000179.3:c.2480A>C