Canonical Allele Identifier: PA2826503814
Gene: SRP72 HGNC NCBI

Linked Data

ClinVar Variation Id: 436861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254651.1:p.Ala64Val
CA2930992
NM_001267722.2:c.191C>T