Canonical Allele Identifier: PA645417685
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312892
ClinVar RCV Id: RCV000259550 RCV000317103 RCV000361426 RCV000374287 RCV001177405 RCV001223055 RCV002338895 RCV002480129 RCV003320153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1676Trp
CA044958
NM_000257.4:c.5026C>T