Canonical Allele Identifier: PA131920
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42961
ClinVar RCV Id: RCV000035854 RCV000769451 RCV002259311 RCV002453300 RCV002477071 RCV000706291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1152Val
CA013725
NM_000257.4:c.3455A>T