Canonical Allele Identifier: PA2825109825
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1929448
ClinVar RCV Id: RCV002618666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Trp438Cys
CA389050879
NM_000257.4:c.1314G>T
CA389050880
NM_000257.4:c.1314G>C