Canonical Allele Identifier: PA658804489
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 524945
ClinVar RCV Id: RCV000628849 RCV003532209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala970Ser
CA389046622
NM_000257.4:c.2908G>T