Canonical Allele Identifier: PA916051846
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 640244
ClinVar RCV Id: RCV000793224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060004.3:p.His361Asn
CA398163026
NM_017534.6:c.1081C>A