Canonical Allele Identifier: PA332598
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135906
ClinVar RCV Id: RCV000123042 RCV002362751
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077071.1:p.Met150Val
CA332595
NM_001083602.3:c.448A>G