Canonical Allele Identifier: PA2825497158
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730790
ClinVar RCV Id: RCV002451799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Leu1126Val
CA374111788
NM_001083603.3:c.3376C>G