Canonical Allele Identifier: PA2825086696
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1757960
ClinVar RCV Id: RCV002382535 RCV003594237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser242Ile
CA346740018
NM_000179.3:c.725G>T