Canonical Allele Identifier: PA131743
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42840
ClinVar RCV Id: RCV000035720 RCV000477379 RCV000617592 RCV001258094 RCV001804758 RCV002496539 RCV003478982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile457Thr
CA010654
NM_000257.4:c.1370T>C