Canonical Allele Identifier: PA296686
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181266
ClinVar RCV Id: RCV000158670 RCV000620277 RCV001183734 RCV001850221 RCV002484978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1603Thr
CA015331
NM_000257.4:c.4807G>A