Canonical Allele Identifier: PA296880
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181379
ClinVar RCV Id: RCV000158852 RCV001306502 RCV002433704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp928Val
CA013062
NM_000257.4:c.2783A>T