Canonical Allele Identifier: PA645382313
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237161
ClinVar RCV Id: RCV000568833 RCV001297702 RCV003998720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp857Asn
CA069199
NM_000179.3:c.2569G>A