Canonical Allele Identifier: PA2825109916
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2767883
ClinVar RCV Id: RCV003588007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala463Ser
CA389050731
NM_000257.4:c.1387G>T