Canonical Allele Identifier: PA2825112229
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2157448
ClinVar RCV Id: RCV003079584 RCV004071840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1091Ser
CA257816463
NM_000257.4:c.3272A>G