Canonical Allele Identifier: PA296618
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181226
ClinVar RCV Id: RCV000223885 RCV000766447 RCV000794278 RCV002453547 RCV003998357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1184Leu
CA013801
NM_000257.4:c.3551A>T