Canonical Allele Identifier: PA2825092235
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587328
ClinVar RCV Id: RCV003350669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser1251Ala
CA346761077
NM_000179.3:c.3751T>G