Canonical Allele Identifier: PA131917
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42959
ClinVar RCV Id: RCV000035852 RCV000172567 RCV000471337 RCV000758075 RCV002453299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1128Thr
CA013661
NM_000257.4:c.3382G>A