Canonical Allele Identifier: PA645381790
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234218
ClinVar RCV Id: RCV000219984 RCV000473229 RCV000985831 RCV003463605 RCV003998608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser753Cys
CA10578102
NM_000179.3:c.2258C>G