Canonical Allele Identifier: PA2826629356
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141327
ClinVar RCV Id: RCV000129804 RCV000204360 RCV000409369 RCV000656905 RCV001375525 RCV003467121 RCV004532553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1205Ala
CA015298
NM_001281492.2:c.3614A>C