Canonical Allele Identifier: PA658680279
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455342
ClinVar RCV Id: RCV000535308 RCV000571023 RCV004003702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile245Val
CA346740050
NM_000179.3:c.733A>G