Canonical Allele Identifier: PA2826633196
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127587
ClinVar RCV Id: RCV000115416 RCV000212684 RCV000819197 RCV003453035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala860Asp
CA013090
NM_001281493.2:c.2579C>A