Canonical Allele Identifier: PA2499230372
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172468
ClinVar RCV Id: RCV001526342 RCV003748348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr185Ile
CA389052557
NM_000257.4:c.554C>T