Canonical Allele Identifier: PA2825108258
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070017
ClinVar RCV Id: RCV004010049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser4Thr
CA389054235
NM_000257.4:c.10T>A