Canonical Allele Identifier: PA2825539346
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_001093582.1:p.His361Asn
CA398163026
NM_001100112.2:c.1081C>A