Canonical Allele Identifier: PA645379170
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232265
ClinVar RCV Id: RCV000215484 RCV001216925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly306Arg
CA10578052
NM_000179.3:c.916G>A
CA346740730
NM_000179.3:c.916G>C