Canonical Allele Identifier: PA658748970
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491937
ClinVar RCV Id: RCV000582580 RCV000808125 RCV004002352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp1107Glu
CA346758673
NM_000179.3:c.3321T>G
CA346758674
NM_000179.3:c.3321T>A