Canonical Allele Identifier: PA2825089707
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2864305
ClinVar RCV Id: RCV003759358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu821Ile
CA346754090
NM_000179.3:c.2461C>A
CA2739274368
NM_000179.3:c.2460_2461delinsAA