Canonical Allele Identifier: PA658680257
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455340
ClinVar RCV Id: RCV000550811 RCV000566216 RCV003327411
ClinVar Variation Id: 847895
ClinVar RCV Id: RCV001051535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln236His
CA346739985
NM_000179.3:c.708A>C
CA346739986
NM_000179.3:c.708A>T