Canonical Allele Identifier: PA658744490
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490027
ClinVar RCV Id: RCV000580368 RCV003593995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys295Thr
CA346740673
NM_000179.3:c.884A>C