Canonical Allele Identifier: PA325798
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43020
ClinVar RCV Id: RCV000035914 RCV000172762 RCV000203136 RCV000254102 RCV000331016 RCV000712360 RCV000758034 RCV000852699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1491Cys
CA015008
NM_000257.4:c.4472C>G