Canonical Allele Identifier: PA1139671307
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 923672
ClinVar RCV Id: RCV001184589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val52Leu
CA389053721
NM_000257.4:c.154G>T
CA389053722
NM_000257.4:c.154G>C